{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4271526009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4158320009,"location":{"name":"Remote"},"metadata":null,"id":4271526009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"271","title":"Accounts Payable Specialist","company_name":"Headlands Research","first_published":"2026-06-03T17:46:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Headlands Research is seeking an experienced Accounts Payable Specialist to join our centralized Accounting team. This fully remote role supports multiple entities across a growing organization and reports directly to the Director of Accounting.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate is highly organized, detail-oriented, and able to work independently with minimal supervision. This position requires strong problem-solving skills, a customer-service mindset, and the ability to quickly learn and become proficient in multiple financial systems. The successful candidate will regularly collaborate with employees across all levels of the organization and serve as a key resource for accounts payable processes, systems, and vendor management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Duties \u0026amp;amp; Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review and process vendor invoices in NetSuite\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and process ACH, wire, and other electronic vendor payments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage vendor payment portals and vendor account setup\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review vendor account statements and reconcile outstanding invoices, payments, and credits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and manage multiple accounts payable email inboxes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process and review employee expense reports through the company\u0026#39;s expense management system\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a superuser for the company\u0026#39;s expense management system, providing user support, training, and troubleshooting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with site and department leaders to obtain invoice and expense approvals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform credit card coding and reconciliations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain vendor records, including W-9s, banking information, and payment details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and file annual 1099s for multiple entities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with reporting, compliance requests, and special projects as assigned\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with the development, documentation, and improvement of AP procedures and internal controls\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Experience:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;4+ years of accounts payable experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience preparing and filing 1099s\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using and supporting an expense management system such as Emburse, Concur, Ramp, Expensify, or similar\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting multiple entities, business units, or locations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of accounts payable processes and controls\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Excel\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to learn, support, and troubleshoot financial systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Preferred Qualifications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with NetSuite\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience processing electronic payments, including ACH and wire transfers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foundational accounting knowledge, including prepaids, fixed assets, and accruals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with NetSuite\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience processing electronic payments, including ACH and wire transfers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foundational accounting knowledge, including prepaids, fixed assets, and accruals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Remote Pay Range.\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$60,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$65,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005121009,"name":"Finance \u0026 Accounting","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4249502009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4145829009,"location":{"name":"Kelowna, British Columbia"},"metadata":null,"id":4249502009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"256","title":"Administrative Coordinator","company_name":"Headlands Research","first_published":"2026-05-15T15:06:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;GENERAL DESCRIPTION\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;Okanagan Clinical Trials is\u0026amp;nbsp;seeking\u0026amp;nbsp;a\u0026amp;nbsp;fulltime\u0026amp;nbsp;Administration Coordinator\u0026amp;nbsp;in Kelowna, BC.\u0026amp;nbsp;Successful applicants\u0026amp;nbsp;will have a positive attitude, a desire to work as efficiently as possible, and excellent communication skills.\u0026amp;nbsp;As\u0026amp;nbsp;Administration Coordinator, you will provide\u0026amp;nbsp;general administrative and clerical support\u0026amp;nbsp;as\u0026amp;nbsp;required,\u0026amp;nbsp;as well as\u0026amp;nbsp;assist in\u0026amp;nbsp;accounting functions such as\u0026amp;nbsp;petty\u0026amp;nbsp;cash\u0026amp;nbsp;maintenance and\u0026amp;nbsp;accounts payable.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;KEY RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO THE FOLLOWING:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Greet\u0026amp;nbsp;clients\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure office is\u0026amp;nbsp;presentable\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Answer, screen, and forward incoming\u0026amp;nbsp;calls\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage patient\u0026amp;nbsp;database\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform client reminder calls, follow-up calls, and scheduling as\u0026amp;nbsp;required\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensuring all Accounts Payable invoices are entered\u0026amp;nbsp;daily\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage occasional accounts receivable\u0026amp;nbsp;invoice\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Process stipends and generate cheque runs and\u0026amp;nbsp;distribution\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform office\u0026amp;nbsp;errands\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Update social\u0026amp;nbsp;media\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Request and reconcile monthly statements from select\u0026amp;nbsp;vendors\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review documents for accuracy and\u0026amp;nbsp;completeness\u0026amp;nbsp;and\u0026amp;nbsp;working on\u0026amp;nbsp;spreadsheets\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide support to the controller and management and perform other duties as\u0026amp;nbsp;assigned\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain historical records by scanning,\u0026amp;nbsp;uploading,\u0026amp;nbsp;and filing\u0026amp;nbsp;documents\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Meeting Minutes / Agenda\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ordering supplies as required\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;EDUCATION, EXPERIENCE AND SKILLS REQUIRED:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of\u0026amp;nbsp;2\u0026amp;nbsp;years\u0026amp;nbsp;experience\u0026amp;nbsp;in accounts payable/ receivable\u0026amp;nbsp;is\u0026amp;nbsp;preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Number and data\u0026amp;nbsp;accuracy\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and\u0026amp;nbsp;superb\u0026amp;nbsp;organizational\u0026amp;nbsp;skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Interpersonal and\u0026amp;nbsp;time\u0026amp;nbsp;management skills,\u0026amp;nbsp;and ability to\u0026amp;nbsp;prioritize\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proficient in\u0026amp;nbsp;Excel, Word, and Outlook\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent at relationship\u0026amp;nbsp;building\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent\u0026amp;nbsp;verbal and written communication skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ability to work well under limited supervision\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Okanagan Clinical Trials is a Headlands Research site. Our clinic specializes in the execution of research studies that hope to advance treatments for many indications including Alzheimer’s disease, migraine, COPD, stress urinary incontinence, celiac disease, diabetes, and more.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Status\u0026lt;/strong\u0026gt;:\u0026amp;nbsp;Full Time / 40 hours per week\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Salary:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$52,000 - $54,000 (Depending on experience)\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Employee benefits\u0026lt;/strong\u0026gt;:\u0026amp;nbsp;Benefits are available\u0026amp;nbsp;after 3-month probationary\u0026amp;nbsp;period.\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule\u0026lt;/strong\u0026gt;:\u0026amp;nbsp;Monday to Friday 8am – 4:30pm\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We thank all applicants for their interest;\u0026amp;nbsp;however, only those selected for an interview will be contacted.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005112009,"name":"Office Support","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004756009,"name":"Canada - Kelowna, BC","location":"Kelowna, British Columbia, Canada","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4173223009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4100192009,"location":{"name":"Riverside, California"},"metadata":null,"id":4173223009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"171","title":"Bilingual Front Desk Medical Receptionist","company_name":"Headlands Research","first_published":"2026-03-05T13:05:54-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt; We are seeking a Front Desk Receptionist to join our clinical research site in Riverside. This pivotal role will involve managing the front desk operations and supporting the administrative tasks for the site. The ideal candidate will demonstrate strong organizational and management skills, high proficiency in technology/computer applications, and a commitment to providing excellent customer service.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Full Time\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026lt;/strong\u0026gt; $20-$23/hr, based on experience\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Riverside, CA (no remote opportunities)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt; Mondays through Fridays, 7:00 AM to 3:30 PM\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Friendly and Collaborative Culture:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Be part of a dynamic team that values collaboration and growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Professional Growth:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Opportunities for advancement in a rapidly growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Comprehensive Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Enjoy a range of medical and dental plans, vision coverage, 401(k) with company match, paid holidays, paid time off, and more.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Greet and assist patients in a friendly and professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage phone calls and schedule appointments efficiently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the reception area is clean, organized, and welcoming.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collect patient information and maintain accurate records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with clinical staff to support operational needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle various administrative tasks as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage office supplies and equipment to ensure operational compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with facility-related expenses to ensure budget adherence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent; certification in medical office administration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience scheduling customer/patient appointments and handling customer/patient phone calls required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within a healthcare environment is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual in english and spanish required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong computer skills with the ability to learn new software systems quickly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication (verbal and written) and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple tasks simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to delivering exceptional customer service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reliable and trustworthy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$20\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$23 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005112009,"name":"Office Support","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4234492009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4136981009,"location":{"name":"Escondido, California"},"metadata":null,"id":4234492009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"238","title":"Bilingual Front Desk Medical Receptionist","company_name":"Headlands Research","first_published":"2026-05-15T09:03:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt; We are seeking a Front Desk Medical Receptionist to join our clinical research site in Escondido. This pivotal role will involve managing the front desk operations and supporting the administrative tasks for the site. The ideal candidate will demonstrate strong organizational and management skills, high proficiency in technology/computer applications, and a commitment to providing excellent customer service.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Full Time\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026lt;/strong\u0026gt; $20-$24/hr, based on experience\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Escondido, CA (no remote opportunities)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt; Full time, Weekday Regular Businses Hours\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Friendly and Collaborative Culture:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Be part of a dynamic team that values collaboration and growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Professional Growth:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Opportunities for advancement in a rapidly growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Comprehensive Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Enjoy a range of medical and dental plans, vision coverage, 401(k) with company match, paid holidays, paid time off, and more.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Greet and assist patients in a friendly and professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage phone calls and schedule appointments efficiently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the reception area is clean, organized, and welcoming.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collect patient information and maintain accurate records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with clinical staff to support operational needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle various administrative tasks as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage office supplies and equipment to ensure operational compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with facility-related expenses to ensure budget adherence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent; certification in medical office administration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience scheduling customer/patient appointments and handling customer/patient phone calls required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within a healthcare environment is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual in english and spanish required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong computer skills with the ability to learn new software systems quickly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication (verbal and written) and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple tasks simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to delivering exceptional customer service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reliable and trustworthy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$20\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$23 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005112009,"name":"Office Support","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4209747009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4122794009,"location":{"name":"Remote"},"metadata":null,"id":4209747009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"216","title":"Budgets \u0026 Contracts Associate","company_name":"Headlands Research","first_published":"2026-04-06T20:56:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are looking for a motivated individual to support the Budget \u0026amp;amp; Contracts team with site clinical trial agreements and related documents, processes, and systems. The Budget \u0026amp;amp; Contracts Associate will communicate regularly with internal and external stakeholders including but not limited to Budget \u0026amp;amp; Contract Managers, Financial teams, Operational leaders, Site Directors, Sponsors and CROs. You will assist with Budget \u0026amp;amp; Contract processes to effectively execute maximum revenue contracts in an assertive timeframe to ensure our sites can be the first to enroll in any given study.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The successful candidate for this role should possess strong and professional communication skills, excellent attention to detail, resourcefulness, the ability to multitask in a fast-paced environment and a “how might we” mentality.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Duties\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain electronic files and related data/system fields for clinical trial contractual agreements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track negotiations and follow-up as needed to ensure timely execution of clinical trial contractual agreements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor group mailbox for actionable items and address or communicate to responsible party accordingly\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in providing accurate and up-to-date status information to the organization as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow up with internal and external stakeholders to move processes forward in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiate and process contractual amendments through full execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initiates and finalizes budgets for federally- funded awarded trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete payment information forms and similar questionnaires\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the periodic review and QC of agreements and related data, including routing CTA documents as required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the organization’s effective use of systems, including holding training and creating presentations to explain workflows and best practices\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp; \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in business, Finance, Life Science and/or equivalent experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Resourceful with the ability to multitask in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High degree of accuracy, organization, and attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate clearly and effectively in a professional manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to successfully work in a “virtual” team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong Microsoft Office suite experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Salesforce and/or LinkSquares a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with clinical trial agreements and budgets a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paralegal experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt; Full Time, Permanent\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Fully Remote\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;0%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt; Monday - Friday, Regular Business Hours\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005118009,"name":"Budgets \u0026 Contracts","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4156263009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4095614009,"location":{"name":"Richmond, British Columbia"},"metadata":null,"id":4156263009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"167","title":"Clinical Research Assistant","company_name":"Headlands Research","first_published":"2026-02-27T13:55:39-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Assistant (non-lab)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Richmond, BC | 🏥 Site Name: Richmond Clinical Trials | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Assistant (RA)\u0026lt;/strong\u0026gt; for our clinical research site Richmond Clinical Trials located in Richmond, BC. As a Research Assistant, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;💼 The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a Clinical Research Assistant, you’ll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution—from subject screening to data entry. Your work will directly contribute to the success of new treatments in development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 4:30pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026lt;/strong\u0026gt; $54,000 - $58,000 *Dependent upon relevant experience, certification, and education.\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Richmond, BC (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Benefits will be included after a 3-month probation period\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1696\u0026quot; data-end=\u0026quot;1801\u0026quot;\u0026gt;Assist research coordinators in \u0026lt;strong data-start=\u0026quot;1728\u0026quot; data-end=\u0026quot;1764\u0026quot;\u0026gt;conducting clinical trial visits\u0026lt;/strong\u0026gt; in compliance with study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1913\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1838\u0026quot;\u0026gt;Collect and record vital signs\u0026lt;/strong\u0026gt;, make study-related phone calls, and document data in electronic systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1916\u0026quot; data-end=\u0026quot;1984\u0026quot;\u0026gt;Support subject \u0026lt;strong data-start=\u0026quot;1932\u0026quot; data-end=\u0026quot;1957\u0026quot;\u0026gt;screening, enrollment\u0026lt;/strong\u0026gt;, and follow-up processes\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1987\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Review and verify study documentation for \u0026lt;strong data-start=\u0026quot;2029\u0026quot; data-end=\u0026quot;2058\u0026quot;\u0026gt;accuracy and completeness\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2063\u0026quot; data-end=\u0026quot;2150\u0026quot;\u0026gt;Maintain close communication with coordinators, investigators, and study participants\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with medical terminology and basic laboratory procedures preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience providing direct hands-on patient care preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical research experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2404\u0026quot; data-end=\u0026quot;2478\u0026quot;\u0026gt;Comfortable using multiple electronic data entry systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2481\u0026quot; data-end=\u0026quot;2586\u0026quot;\u0026gt;Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2589\u0026quot; data-end=\u0026quot;2686\u0026quot;\u0026gt;Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2689\u0026quot; data-end=\u0026quot;2746\u0026quot;\u0026gt;Passion for improving patient outcomes through research\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004755009,"name":"Canada - Richmond, BC","location":"Richmond, British Columbia, Canada","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4227754009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4133273009,"location":{"name":"Rolling Hills Estates, California"},"metadata":null,"id":4227754009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"236","title":"Clinical Research Assistant/Laboratory Technician","company_name":"Headlands Research","first_published":"2026-04-21T14:08:21-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p data-start=\u0026quot;167\u0026quot; data-end=\u0026quot;247\u0026quot;\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Rolling Hills Estates, CA\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;500\u0026quot; data-end=\u0026quot;503\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;506\u0026quot; data-end=\u0026quot;558\u0026quot;\u0026gt;Peninsula Research Associates\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;558\u0026quot; data-end=\u0026quot;561\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Full-Time | Monday through Friday | 8:00am - 5:00pm\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;Launch Your Career in Healthcare \u0026amp;amp; Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;299\u0026quot; data-end=\u0026quot;612\u0026quot;\u0026gt;Are you a recent graduate looking to gain hands-on experience in healthcare, clinical research, or laboratory sciences? This is an exciting opportunity to build real-world skills, work alongside experienced professionals, and contribute to meaningful research that impacts patient care and scientific advancement.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;614\u0026quot; data-end=\u0026quot;949\u0026quot;\u0026gt;As a Laboratory Technician, you’ll play a critical role in supporting lab operations, handling biological samples, and ensuring accurate data collection. Whether you\u0026#39;re planning a future in healthcare, research, or advanced clinical roles, this position offers a strong foundation and valuable exposure to a fast-paced lab environment.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;951\u0026quot; data-end=\u0026quot;954\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;xti9y5\u0026quot; data-start=\u0026quot;956\u0026quot; data-end=\u0026quot;976\u0026quot;\u0026gt;What You’ll Do\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collect, process, and prepare biological specimens (e.g., blood, urine, saliva) according to protocol and laboratory guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Package and ship samples to central and specialty laboratories with accurate and timely documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform point-of-care testing, including urine pregnancy tests, drug/cotinine screens, and alcohol testing\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately record laboratory data and maintain source documentation (paper and electronic) in real time during processing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and organize laboratory kits and supplies ahead of study visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain laboratory inventory, including stocking and tracking supplies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure strict adherence to safety, infection control, and handling procedures for biological specimens\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a clean, organized, and inspection-ready laboratory environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review documentation for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research staff with basic data entry, lab-related queries, and study-related tasks as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1487\u0026quot; data-end=\u0026quot;1490\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1f5kc01\u0026quot; data-start=\u0026quot;1492\u0026quot; data-end=\u0026quot;1524\u0026quot;\u0026gt;What Makes You a Great Fit\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and ability to follow step-by-step procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work efficiently in a fast-paced environment with changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic knowledge of laboratory procedures and specimen handling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear communication and ability to work both independently and as part of a team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional, reliable, and eager to learn\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willing to be trained in other Research Assistant tasks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2035\u0026quot; data-end=\u0026quot;2038\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Qualifications\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2393\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xrynm\u0026quot; data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2100\u0026quot;\u0026gt;High School Diploma or GED required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;Associate’s or Bachelor’s degree in a science-related field preferred (Biology, Chemistry, Health Sciences, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;At least 1 year of experience processing or handling laboratory specimens required (academic, clinical, hospital, lab, or similar setting)\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;Phlebotomy experience preferred but not required (willingness to train or obtain certification is a plus)\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;Experience working with human biological samples preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;Basic computer skills (Microsoft Word, Excel, Outlook)\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8c3v0r\u0026quot; data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2218\u0026quot;\u0026gt;Ability to lift up to 50 lbs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2395\u0026quot; data-end=\u0026quot;2398\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;iyhmpw\u0026quot; data-start=\u0026quot;2400\u0026quot; data-end=\u0026quot;2441\u0026quot;\u0026gt;Why This Role is a Great First Step\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2442\u0026quot; data-end=\u0026quot;2766\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;165k4uh\u0026quot; data-start=\u0026quot;2442\u0026quot; data-end=\u0026quot;2511\u0026quot;\u0026gt;Gain hands-on experience with lab procedures and clinical samples\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;p3c0xk\u0026quot; data-start=\u0026quot;2512\u0026quot; data-end=\u0026quot;2595\u0026quot;\u0026gt;Build foundational skills for careers in healthcare, research, or biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;jrp2fy\u0026quot; data-start=\u0026quot;2596\u0026quot; data-end=\u0026quot;2677\u0026quot;\u0026gt;Work in a professional environment with mentorship and learning opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;12brg8z\u0026quot; data-start=\u0026quot;2678\u0026quot; data-end=\u0026quot;2766\u0026quot;\u0026gt;Make a tangible impact by supporting research that advances science and patient care\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2768\u0026quot; data-end=\u0026quot;2771\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2773\u0026quot; data-end=\u0026quot;2928\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;If you\u0026#39;re looking to turn your academic background into real-world experience and start a meaningful career in healthcare, this is a strong place to begin.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$22\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$25 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; 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data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005110009,"name":"Clinical: Laboratory","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4234648009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4137069009,"location":{"name":"Atlanta, Georgia; Baltimore, Maryland; Brownsville, Texas; Chesterfield, Missouri; Detroit, Michigan; El Paso, Texas; Escondido, California; Kelowna, British Columbia; Lake Worth, Florida; Maplewood, Minnesota; Myrtle Beach, South Carolina; Orlando, Florida; Plymouth, Massachusetts; Portland, Oregon; Richmond, British Columbia; Riverside, California; Rolling Hills Estates, California; San Diego, California; San Juan, Puerto Rico; Scottsdale, Arizona; Springfield, Missouri; Toronto, Ontario; Wilmington, North Carolina"},"metadata":null,"id":4234648009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"239","title":"Clinical Research Assistant Opportunities – Multiple Locations Nationwide","company_name":"Headlands Research","first_published":"2026-04-28T15:47:49-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3 style=\u0026quot;text-align: left;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;588\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1bshr1k\u0026quot; data-start=\u0026quot;202\u0026quot; data-end=\u0026quot;232\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;205\u0026quot; data-end=\u0026quot;230\u0026quot;\u0026gt;About the Opportunity\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;233\u0026quot; data-end=\u0026quot;379\u0026quot;\u0026gt;We’re always interested in connecting with individuals who are curious about, experienced in, or eager to grow their careers in clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;381\u0026quot; data-end=\u0026quot;630\u0026quot;\u0026gt;This general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;632\u0026quot; data-end=\u0026quot;953\u0026quot;\u0026gt;Research Assistants play a critical role in supporting clinical trials and bridging the gap between research and patient care. This is an ideal opportunity for individuals with patient-care, lab, academic, or research experience who are looking to transition into a clinical research role and gain hands-on clinical exposure.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ksuq6e\u0026quot; data-start=\u0026quot;960\u0026quot; data-end=\u0026quot;980\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ksuq6e\u0026quot; data-start=\u0026quot;960\u0026quot; data-end=\u0026quot;980\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;963\u0026quot; data-end=\u0026quot;978\u0026quot;\u0026gt;Our Process\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;981\u0026quot; data-end=\u0026quot;1358\u0026quot;\u0026gt;When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming Research Assistant opportunities. As new roles open, we proactively match candidates based on location preference, education, experience, and career interests. If there’s a strong fit, a member of our team will reach out to start the conversation.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1942f6b\u0026quot; data-start=\u0026quot;1365\u0026quot; data-end=\u0026quot;1428\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1942f6b\u0026quot; data-start=\u0026quot;1365\u0026quot; data-end=\u0026quot;1428\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1368\u0026quot; data-end=\u0026quot;1426\u0026quot;\u0026gt;What Research Assistant Roles Look Like at Our Company\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1429\u0026quot; data-end=\u0026quot;1654\u0026quot;\u0026gt;Research Assistants support the execution of clinical trials by assisting with study visits, preparing study materials, collecting and organizing data, and helping ensure studies run smoothly and in compliance with protocols.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1656\u0026quot; data-end=\u0026quot;1993\u0026quot;\u0026gt;This role offers direct exposure to patient interactions, clinical workflows, and regulatory processes. Research Assistants work closely with Clinical Research Coordinators, investigators, and patients, gaining valuable experience that can serve as a strong foundation for advancement into Clinical Research Coordinator roles and beyond.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1995\u0026quot; data-end=\u0026quot;2149\u0026quot;\u0026gt;Responsibilities may vary depending on experience level and site needs but are designed to provide meaningful, hands-on learning and growth opportunities.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;iw5hjp\u0026quot; data-start=\u0026quot;2156\u0026quot; data-end=\u0026quot;2186\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;iw5hjp\u0026quot; data-start=\u0026quot;2156\u0026quot; data-end=\u0026quot;2186\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2159\u0026quot; data-end=\u0026quot;2184\u0026quot;\u0026gt;Who We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;2187\u0026quot; data-end=\u0026quot;2233\u0026quot;\u0026gt;We welcome interest from candidates who bring:\u0026lt;/p\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2235\u0026quot; data-end=\u0026quot;2852\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;18ln0ve\u0026quot; data-start=\u0026quot;2235\u0026quot; data-end=\u0026quot;2369\u0026quot;\u0026gt;A bachelor’s or master\u0026#39;s degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1rnu1lm\u0026quot; data-start=\u0026quot;2370\u0026quot; data-end=\u0026quot;2518\u0026quot;\u0026gt;Hands-on experience in lab work, research projects, or clinical environments\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;jq1vpl\u0026quot; data-start=\u0026quot;2519\u0026quot; data-end=\u0026quot;2596\u0026quot;\u0026gt;Strong attention to detail and the ability to follow structured protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1y9ewk5\u0026quot; data-start=\u0026quot;2597\u0026quot; data-end=\u0026quot;2652\u0026quot;\u0026gt;Excellent organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;z3rpqd\u0026quot; data-start=\u0026quot;2653\u0026quot; data-end=\u0026quot;2742\u0026quot;\u0026gt;Clear communication skills and a desire to work directly with patients and care teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;aydp4l\u0026quot; data-start=\u0026quot;2743\u0026quot; data-end=\u0026quot;2852\u0026quot;\u0026gt;A positive team-based attitude and approach\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;aydp4l\u0026quot; data-start=\u0026quot;2743\u0026quot; data-end=\u0026quot;2852\u0026quot;\u0026gt;Prior clinical research experience is a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1hlzz4l\u0026quot; data-start=\u0026quot;2941\u0026quot; data-end=\u0026quot;3008\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1hlzz4l\u0026quot; data-start=\u0026quot;2941\u0026quot; data-end=\u0026quot;3008\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2944\u0026quot; data-end=\u0026quot;3006\u0026quot;\u0026gt;Why Start or Grow Your Career in Clinical Research with Us\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul data-start=\u0026quot;3009\u0026quot; data-end=\u0026quot;3603\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;hx86iv\u0026quot; data-start=\u0026quot;3009\u0026quot; data-end=\u0026quot;3104\u0026quot;\u0026gt;A strong entry point into clinical research with exposure to both research and patient care\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;y7jzbr\u0026quot; data-start=\u0026quot;3105\u0026quot; data-end=\u0026quot;3212\u0026quot;\u0026gt;Hands-on experience supporting clinical trials and working alongside experienced CRCs and investigators\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;y9hfb1\u0026quot; data-start=\u0026quot;3213\u0026quot; data-end=\u0026quot;3312\u0026quot;\u0026gt;Opportunities to learn Good Clinical Practice (GCP), regulatory processes, and study operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;btzd64\u0026quot; data-start=\u0026quot;3421\u0026quot; data-end=\u0026quot;3510\u0026quot;\u0026gt;Clear pathways for growth into Clinical Research Coordinator and other roles\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;yp7o7k\u0026quot; data-start=\u0026quot;3511\u0026quot; data-end=\u0026quot;3603\u0026quot;\u0026gt;The opportunity to contribute to developing new treatments that improve patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ey90ou\u0026quot; data-start=\u0026quot;3610\u0026quot; data-end=\u0026quot;3651\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ey90ou\u0026quot; data-start=\u0026quot;3610\u0026quot; data-end=\u0026quot;3651\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;3613\u0026quot; data-end=\u0026quot;3649\u0026quot;\u0026gt;Ready to Start the Conversation?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;3652\u0026quot; data-end=\u0026quot;3827\u0026quot;\u0026gt;Whether you’re coming from a lab, academic research, or early clinical background and are looking to take the next step into a more patient-focused role, we’d love to connect.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;3829\u0026quot; data-end=\u0026quot;4029\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;Apply here to be considered for current and future Research Assistant opportunities. Our Talent Acquisition team will reach out as roles become available that align with your background and interests.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;588\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004740009,"name":"Arizona - Scottsdale","location":"Scottsdale, Arizona, United States","child_ids":[],"parent_id":4004735009},{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004756009,"name":"Canada - Kelowna, BC","location":"Kelowna, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004755009,"name":"Canada - Richmond, BC","location":"Richmond, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004757009,"name":"Canada - Toronto, ON","location":"Toronto, Ontario, Canada","child_ids":[],"parent_id":4004734009},{"id":4004750009,"name":"Florida - Lake Worth","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004751009,"name":"Florida - Orlando","location":"Orlando, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009},{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009},{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009},{"id":4004745009,"name":"Michigan - Detroit","location":"Southfield, Michigan, United States","child_ids":[],"parent_id":4004734009},{"id":4004747009,"name":"Minnesota - Twin Cities","location":null,"child_ids":[],"parent_id":4004734009},{"id":4004744009,"name":"Missouri - Springfield","location":"Springfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004754009,"name":"North Carolina - Wilmington","location":"Wilmington, North Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004741009,"name":"Oregon - Portland","location":"Portland, Oregon, United States","child_ids":[],"parent_id":4004735009},{"id":4007276009,"name":"Puerto Rico - San Juan","location":"San Juan, Puerto Rico","child_ids":[],"parent_id":4004733009},{"id":4004753009,"name":"South Carolina - Myrtle Beach","location":"Myrtle Beach, South Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009},{"id":4004746009,"name":"Texas - El Paso","location":"El Paso, Texas, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4091997009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4062297009,"location":{"name":"Lake Worth, Florida"},"metadata":null,"id":4091997009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"113","title":"Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-01-07T09:08:06-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Lake Worth, FL | 🏥 Site Name: JEM Research Institute | 🕒 Full-Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt; for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase II-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:30am - 4:30pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Clinical Research Manager\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;💼 \u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;🚀\u0026amp;nbsp;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation to study close-out\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage subject recruitment, informed consent, and retention strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely data entry and resolution of EDC queries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Report and follow up on all adverse events, serious adverse events, and deviations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Required:\u0026lt;/strong\u0026gt; High school diploma or GED\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;1 year\u0026lt;/strong\u0026gt; of experience as a Clinical Research Coordinator OR\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;2 years\u0026lt;/strong\u0026gt; of experience as a Research Assistant in Clinical Research\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in medical terminology and clinical documentation practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, verbal, and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized, detail-oriented, and capable of managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and other clinical research systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual (English/Spanish) is strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;📬 \u0026lt;strong\u0026gt;Apply now\u0026lt;/strong\u0026gt; to become a part of a team that’s changing the future of healthcare—one trial at a time.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004750009,"name":"Florida - Lake Worth","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4218187009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4127709009,"location":{"name":"Baltimore, Maryland"},"metadata":null,"id":4218187009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"225","title":"Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-04-13T13:50:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Pikesville, MD | 🏥 Site Name: Headlands Research - Pharmasite | 🕒 Full-Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt; for our clinical research site located in Pikesville, MD. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 5:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Pikesville, MD (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;💼 \u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;🚀 \u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation to study close-out\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage subject recruitment, informed consent, and retention strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely data entry and resolution of EDC queries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Report and follow up on all adverse events, serious adverse events, and deviations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required OR licensed as a Licensed Practical Nurse (LPN) or higher\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Clinical Research Coordinator preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in medical terminology and clinical documentation practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, verbal, and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized, detail-oriented, and capable of managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and other clinical research systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;📬 \u0026lt;strong\u0026gt;Apply now\u0026lt;/strong\u0026gt; to become a part of a team that’s changing the future of healthcare—one trial at a time.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4236902009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4138432009,"location":{"name":"Lake Worth, Florida"},"metadata":null,"id":4236902009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"241","title":"Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-04-30T13:23:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Lake Worth, FL | 🏥 Site Name: JEM Research Institute | 🕒 Full-Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt; for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase II-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:30am - 4:30pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Clinical Research Manager\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;💼 \u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;🚀 \u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation to study close-out\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage subject recruitment, informed consent, and retention strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely data entry and resolution of EDC queries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Report and follow up on all adverse events, serious adverse events, and deviations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;🎓 \u0026lt;strong\u0026gt;Education \u0026amp;amp; Experience Requirements\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Required:\u0026lt;/strong\u0026gt; High school diploma or GED\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;1 year\u0026lt;/strong\u0026gt; of experience as a Clinical Research Coordinator OR\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;2 years\u0026lt;/strong\u0026gt; of experience as a Research Assistant in Clinical Research\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;🧠 \u0026lt;strong\u0026gt;Skills \u0026amp;amp; Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in medical terminology and clinical documentation practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, verbal, and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized, detail-oriented, and capable of managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and other clinical research systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual (English/Spanish) is strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;📬 \u0026lt;strong\u0026gt;Apply now\u0026lt;/strong\u0026gt; to become a part of a team that’s changing the future of healthcare—one trial at a time.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004750009,"name":"Florida - Lake Worth","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4237760009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4138909009,"location":{"name":"Brownsville, Texas"},"metadata":null,"id":4237760009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"242","title":"Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-05-14T11:30:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Brownsville, TX | 🏥 Site Name: Headlands Research Brownsville | 🕒 Full-Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Coordinator (CRC)\u0026lt;/strong\u0026gt; for our clinical research site located in Brownsville, TX. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 5:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Brownsville, TX (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;💼 \u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;🚀 \u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;You’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation to study close-out\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage subject recruitment, informed consent, and retention strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely data entry and resolution of EDC queries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Report and follow up on all adverse events, serious adverse events, and deviations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required OR licensed as a Licensed Practical Nurse (LPN) or higher\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Clinical Research Coordinator preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in medical terminology and clinical documentation practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal, verbal, and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized, detail-oriented, and capable of managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and other clinical research systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;📬 \u0026lt;strong\u0026gt;Apply now\u0026lt;/strong\u0026gt; to become a part of a team that’s changing the future of healthcare—one trial at a time.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4113751009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4077458009,"location":{"name":"Plymouth, MA"},"metadata":null,"id":4113751009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"136","title":"Clinical Research Coordinator - General Interest","company_name":"Headlands Research","first_published":"2026-01-29T09:30:37-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 style=\u0026quot;text-align: left;\u0026quot;\u0026gt;We’re always interested in connecting with Clinical Research Coordinators who would like to be considered for future roles at our Eastern Massachusetts location.\u0026lt;/h3\u0026gt;\n\u0026lt;h3 style=\u0026quot;text-align: left;\u0026quot;\u0026gt;Although there is no immediate opening, applications submitted here are reviewed by our team and actively used to pipeline candidates for upcoming opportunities. If a role becomes available that aligns with your background, we’ll be in touch.\u0026lt;/h3\u0026gt;\n\u0026lt;h1\u0026gt;\u0026amp;nbsp;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif;\u0026quot;\u0026gt; \u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Plymouth, MA | 🏥 Site Name: Headlands Research Eastern Massachusetts | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Headlands Research Eastern Massachusetts is a leading clinical trial research site focusing on the care of patients and their families living with neurodegenerative diseases, memory and movement disorders. The Site is an adult outpatient neurology treatment clinic and research center. Dr. Marks is on staff at the Beth Israel Lahey Health Hospital system in Plymouth, MA. The Site is also involved in numerous clinical trials in conjunction with various pharmaceutical, imaging and NIH sponsors.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Mondays through Fridays, 8:00am - 5:00pm\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Onsite in Plymouth, MA (no capabilities for remote or hybrid work)\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Site Manager\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Pay Range: \u0026lt;/strong\u0026gt;Competitive and negotiable; based on years of experience as a CRC in clinical research trials.\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;💼 \u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Competitive pay + annual performance incentives\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Medical, dental, and vision insurance\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;401(k) plan with company match\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr\u0026gt;\n\u0026lt;h2\u0026gt;🚀 \u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Y\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif;\u0026quot;\u0026gt;ou’ll be part of a growing, mission-driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Responsibilities:\u0026lt;/span\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation to study close-out\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention strategies\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Ensure timely data entry and resolution of EDC queries\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Report and follow up on all adverse events, serious adverse events, and deviations\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Requirements:\u0026lt;/span\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif;\u0026quot;\u0026gt;High school diploma or GED required; Bachelor\u0026#39;s Degree preferred\u0026lt;/span\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot;\u0026gt;Industry-sponsored trial experience strongly preferred (vaccine study experience a plus)\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;At least one full year of experience coordinating clinical trials phases 1-4 required\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Previous hands-on clinical experience caring for patients suffering from neurodegenerative diseases highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Familiarity with electronic data capture (EDC), IVRS, and other trial platforms\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation practices\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Strong interpersonal, verbal, and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Organized, detail-oriented, and capable of managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Proficient in Microsoft Office and other clinical research systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-family: helvetica, arial, sans-serif; font-size: 12pt;\u0026quot; data-teams=\u0026quot;true\u0026quot;\u0026gt;📬 \u0026lt;strong\u0026gt;Apply now\u0026lt;/strong\u0026gt; to become a part of a team that’s changing the future of healthcare—one trial at a time.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4240283009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4140400009,"location":{"name":"San Diego, California"},"metadata":null,"id":4240283009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"247","title":"Clinical Research Coordinator I","company_name":"Headlands Research","first_published":"2026-05-06T10:37:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. Together with Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Want to be a part of a growing company that’s making a difference in our world? Look no further than Artemis Institute for Clinical Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A range of PPO and HMO medical plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PPO and HMO dental plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vision coverage, long term disability plan, and life/AD\u0026amp;amp;D coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401k plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid holidays and paid time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A welcoming work environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;We’re looking for a bright, talented new team member to be a part of our story. Check out this current opening and if you think you may be a fit for the role, please apply.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Artemis is looking for a Clinical Research Coordinator for the San Diego office. Under the supervision of the Site Director, the Clinical Research Coordinator I is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Clinical Research Coordinator I manages study conduct from planning through study closeout.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Full Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay Range\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;$27 - $32/hr\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Diego-no remote work\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;0%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Monday \u0026amp;amp; Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Duties/Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Clinical Research Coordinator II (CRCs)/Sr. CRCs in all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and supporting monitoring visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with lab draws, processing and shipping\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s Degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum one to two (1-2) years of experience as a Clinical Research Coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical assistant or phlebotomist required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;job__pay-ranges\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4238114009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4139124009,"location":{"name":"San Diego, California"},"metadata":null,"id":4238114009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"243","title":"Clinical Research Coordinator II","company_name":"Headlands Research","first_published":"2026-05-06T10:42:09-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Company\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. Together with Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Want to be a part of a growing company that’s making a difference in our world? Look no further than Artemis Institute for Clinical Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A range of PPO and HMO medical plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PPO and HMO dental plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vision coverage, long term disability plan, and life/AD\u0026amp;amp;D coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401k plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid holidays and paid time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A welcoming work environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;We’re looking for a bright, talented new team member to be a part of our story. Check out this current opening and if you think you may be a fit for the role, please apply.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Artemis is looking for a Clinical Research Coordinator for the San Diego office. Under the supervision of the Site Director, the Clinical Research Coordinator II is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Clinical Research Coordinator I manages study conduct from planning through study closeout.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Full Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay Range\u0026lt;em\u0026gt;:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; $70,000 - $75,000/hr\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;San Diego-no remote work\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;0%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Monday \u0026amp;amp; Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Duties/Responsibilities \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with lab draws, processing and shipping\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s Degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum three plus (3+) years of experience as a Clinical Research Coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical assistant or phlebotomist required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$70,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$75,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. 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As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. 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The Headlands Research Scottsdale team conducts trials in multiple therapeutic areas, including but not limited to CNS, Psych, Musculoskeletal, Addiction, Healthy Volunteers, etc. They are known for their integration of technology to streamline processes for their Sponsor/CRO partners and most importantly, subjects.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2096\u0026quot; data-end=\u0026quot;2099\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2104\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced CRCs Choose Us\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2145\u0026quot; data-end=\u0026quot;2212\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2251\u0026quot;\u0026gt;Multi-disciplinary collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with seasoned investigators and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2303\u0026quot; data-end=\u0026quot;2346\u0026quot;\u0026gt;Strong operational support and clear SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2349\u0026quot; data-end=\u0026quot;2420\u0026quot;\u0026gt;Exposure to complex, meaningful studies—not just high-volume turnover\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2487\u0026quot; data-end=\u0026quot;2555\u0026quot;\u0026gt;Backing of a growing research network with resources and stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for CRCs who enjoy\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2595\u0026quot; data-end=\u0026quot;2619\u0026quot;\u0026gt;owning their studies\u0026lt;/strong\u0026gt;, working with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2634\u0026quot; data-end=\u0026quot;2653\u0026quot;\u0026gt;competent teams\u0026lt;/strong\u0026gt;, and being trusted to execute with precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Provide the highest level of care for study patients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Deliver excellent customer service to pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation through close-out\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention activities\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Ensure timely EDC data entry and resolution of queries\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Report and follow up on AEs, SAEs, and protocol deviations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Collaborate with investigators, sponsors/CROs, labs, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain regulatory documentation and ensure training compliance for amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Mentor and coach site staff in order to further enhance quality and to best serve our volunteers\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;At least 4-5 years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Experience with EDC, IVRS, and clinical research platforms\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong organizational skills with the ability to manage multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Clear, professional verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Comfortable working onsite in a collaborative, clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4906\u0026quot; data-end=\u0026quot;4909\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4911\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4914\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;CRCs who want\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4959\u0026quot; data-end=\u0026quot;5001\u0026quot;\u0026gt;structure, support, and accountability\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those interested in taking the next step in managing people\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5030\u0026quot; data-end=\u0026quot;5053\u0026quot;\u0026gt;teamwork over silos\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Coordinators who care about data quality, patient experience, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those ready to grow within a stable, well-established research site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5210\u0026quot; data-end=\u0026quot;5213\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;📬\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5218\u0026quot; data-end=\u0026quot;5233\u0026quot;\u0026gt;Apply today\u0026lt;/strong\u0026gt; if you’re looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004740009,"name":"Arizona - Scottsdale","location":"Scottsdale, Arizona, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4227142009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4132930009,"location":{"name":"Rolling Hills Estates, California"},"metadata":null,"id":4227142009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"235","title":"Clinical Research Coordinator I/II","company_name":"Headlands Research","first_published":"2026-05-06T14:08:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;668\u0026quot; data-end=\u0026quot;792\u0026quot;\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;671\u0026quot; data-end=\u0026quot;687\u0026quot;\u0026gt;Rolling Hills Estates, CA\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;687\u0026quot; data-end=\u0026quot;690\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;693\u0026quot; data-end=\u0026quot;748\u0026quot;\u0026gt;Peninsula Research Associates (a Headlands Research site)\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;748\u0026quot; data-end=\u0026quot;751\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;754\u0026quot; data-end=\u0026quot;792\u0026quot;\u0026gt;Full-Time | Monday through Friday | Onsite (no opportunities for hybrid or remote)\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;794\u0026quot; data-end=\u0026quot;876\u0026quot;\u0026gt;For experienced CRCs looking for stability, collaboration, and meaningful work\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;877\u0026quot; data-end=\u0026quot;1122\u0026quot;\u0026gt;If you’re an experienced Clinical Research Coordinator I, or II who values \u0026lt;strong data-start=\u0026quot;943\u0026quot; data-end=\u0026quot;1054\u0026quot;\u0026gt;strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance\u0026lt;/strong\u0026gt;, Peninsula Research Associates may be the right next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;Our Rolling Hills Estates site is known for its \u0026lt;strong data-start=\u0026quot;1159\u0026quot; data-end=\u0026quot;1235\u0026quot;\u0026gt;depth of experience, thoughtful study execution, and team-based approach\u0026lt;/strong\u0026gt; to clinical research—particularly in vaccines, immunology and allergy studies.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1325\u0026quot; data-end=\u0026quot;1328\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1330\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1333\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;About Peninsula Research Associates\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;Peninsula Research Associates (PRA) is dedicated to advancing medical treatments through the use of innovative techniques and increasing awareness. PRA has achieved significant study results in allergy, asthma, vaccines, otitis media and sinusitis treatment and has earned a reputation for conducting quality research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1878\u0026quot; data-end=\u0026quot;2094\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2096\u0026quot; data-end=\u0026quot;2099\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2104\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced CRCs Choose PRA\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2145\u0026quot; data-end=\u0026quot;2212\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2251\u0026quot;\u0026gt;Multi-disciplinary collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with seasoned investigators and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2303\u0026quot; data-end=\u0026quot;2346\u0026quot;\u0026gt;Strong operational support and clear SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2349\u0026quot; data-end=\u0026quot;2420\u0026quot;\u0026gt;Exposure to complex, meaningful studies—not just high-volume turnover\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2423\u0026quot; data-end=\u0026quot;2484\u0026quot;\u0026gt;A site with long-standing credibility and research maturity\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2487\u0026quot; data-end=\u0026quot;2555\u0026quot;\u0026gt;Backing of a growing research network with resources and stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for CRCs who enjoy\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2595\u0026quot; data-end=\u0026quot;2619\u0026quot;\u0026gt;owning their studies\u0026lt;/strong\u0026gt;, working with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2634\u0026quot; data-end=\u0026quot;2653\u0026quot;\u0026gt;competent teams\u0026lt;/strong\u0026gt;, and being trusted to execute with precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;3104\u0026quot; data-end=\u0026quot;3175\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;3177\u0026quot; data-end=\u0026quot;3180\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;3182\u0026quot; data-end=\u0026quot;3203\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;3185\u0026quot; data-end=\u0026quot;3203\u0026quot;\u0026gt;What You’ll Do\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;3262\u0026quot; data-end=\u0026quot;3353\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation through close-out\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3356\u0026quot; data-end=\u0026quot;3459\u0026quot;\u0026gt;Conduct subject visits and ensure accurate, timely documentation in compliance with ALCOA-C standards\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3462\u0026quot; data-end=\u0026quot;3563\u0026quot;\u0026gt;Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3566\u0026quot; data-end=\u0026quot;3638\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention activities\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3641\u0026quot; data-end=\u0026quot;3697\u0026quot;\u0026gt;Ensure timely EDC data entry and resolution of queries\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3700\u0026quot; data-end=\u0026quot;3760\u0026quot;\u0026gt;Report and follow up on AEs, SAEs, and protocol deviations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3763\u0026quot; data-end=\u0026quot;3836\u0026quot;\u0026gt;Collaborate with investigators, sponsors/CROs, labs, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3839\u0026quot; data-end=\u0026quot;3914\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3917\u0026quot; data-end=\u0026quot;4010\u0026quot;\u0026gt;Maintain regulatory documentation and ensure training compliance for amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4013\u0026quot; data-end=\u0026quot;4100\u0026quot;\u0026gt;Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4103\u0026quot; data-end=\u0026quot;4180\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4183\u0026quot; data-end=\u0026quot;4275\u0026quot;\u0026gt;Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4277\u0026quot; data-end=\u0026quot;4280\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4282\u0026quot; data-end=\u0026quot;4311\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4285\u0026quot; data-end=\u0026quot;4311\u0026quot;\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4314\u0026quot; data-end=\u0026quot;4380\u0026quot;\u0026gt;High school diploma or GED required; Bachelor’s degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-weight: bold;\u0026quot; data-start=\u0026quot;4383\u0026quot; data-end=\u0026quot;4478\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;At least one full year of experience coordinating multiple Phase 2–4 industry-sponsored clinical trials required\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-weight: bold;\u0026quot; data-start=\u0026quot;4481\u0026quot; data-end=\u0026quot;4562\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Experience with regulatory, patient visits, consenting, interacting directly with sponsors, and scheduling patient visits required\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-weight: bold;\u0026quot; data-start=\u0026quot;4481\u0026quot; data-end=\u0026quot;4562\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Heavily prefer those who are trained and experienced in phlebotomy\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4481\u0026quot; data-end=\u0026quot;4562\u0026quot;\u0026gt;Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4565\u0026quot; data-end=\u0026quot;4625\u0026quot;\u0026gt;Experience with EDC, IVRS, and clinical research platforms\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;4691\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4694\u0026quot; data-end=\u0026quot;4768\u0026quot;\u0026gt;Strong organizational skills with the ability to manage multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4771\u0026quot; data-end=\u0026quot;4832\u0026quot;\u0026gt;Clear, professional verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4835\u0026quot; data-end=\u0026quot;4904\u0026quot;\u0026gt;Comfortable working onsite in a collaborative, clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4906\u0026quot; data-end=\u0026quot;4909\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4911\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4914\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;CRCs who want\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4959\u0026quot; data-end=\u0026quot;5001\u0026quot;\u0026gt;structure, support, and accountability\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5006\u0026quot; data-end=\u0026quot;5055\u0026quot;\u0026gt;Professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5030\u0026quot; data-end=\u0026quot;5053\u0026quot;\u0026gt;teamwork over silos\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5058\u0026quot; data-end=\u0026quot;5136\u0026quot;\u0026gt;Coordinators who care about data quality, patient experience, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5139\u0026quot; data-end=\u0026quot;5208\u0026quot;\u0026gt;Those ready to grow within a stable, well-established research site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5210\u0026quot; data-end=\u0026quot;5213\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;📬\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5218\u0026quot; data-end=\u0026quot;5233\u0026quot;\u0026gt;Apply today\u0026lt;/strong\u0026gt;\u0026amp;nbsp;if you’re looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$70,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$80,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4194529009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4114525009,"location":{"name":"Atlanta, Georgia; Baltimore, Maryland; Brownsville, Texas; Chesterfield, Missouri; Detroit, Michigan; El Paso, Texas; Escondido, California; Kelowna, British Columbia; Lake Worth, Florida; Maplewood, Minnesota; Myrtle Beach, South Carolina; Orlando, Florida; Plymouth, Massachusetts; Portland, Oregon; Richmond, British Columbia; Riverside, California; Rolling Hills Estates, California; San Diego, California; San Juan, Puerto Rico; Scottsdale, Arizona; Springfield, Missouri; Toronto, Ontario; Wilmington, North Carolina"},"metadata":null,"id":4194529009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"200","title":"Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide","company_name":"Headlands Research","first_published":"2026-04-27T15:55:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3 style=\u0026quot;text-align: left;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;588\u0026quot;\u0026gt;About the Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We’re always interested in connecting with individuals who are curious about, experienced in, or eager to begin a career in clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Coordinators are at the heart of our work. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1244\u0026quot; data-end=\u0026quot;1247\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1249\u0026quot; data-end=\u0026quot;1294\u0026quot;\u0026gt;Our Process\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1339\u0026quot; data-end=\u0026quot;1755\u0026quot;\u0026gt;When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming CRC opportunities. As new roles open, we proactively match candidates based on location preference, education, experience, and career interests. If there’s a strong fit, a member of our team will reach out to start the conversation.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1757\u0026quot; data-end=\u0026quot;1760\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1762\u0026quot; data-end=\u0026quot;1810\u0026quot;\u0026gt;What CRC Roles Look Like at Our Company\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Coordinators support the day-to-day execution of clinical trials. This includes working directly with patients, coordinating study visits, collecting and managing data, and ensuring studies are conducted in compliance with protocols and regulatory requirements.\u0026amp;nbsp;CRCs work closely with investigators, patients, and cross-functional teams, gaining exposure to a wide range of therapeutic areas and research processes. Roles may vary based on experience level and site needs, with opportunities to grow and take on increasing responsibility over time.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2351\u0026quot; data-end=\u0026quot;2354\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2356\u0026quot; data-end=\u0026quot;2380\u0026quot;\u0026gt;Who We’re Looking For\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;2382\u0026quot; data-end=\u0026quot;2428\u0026quot;\u0026gt;We welcome interest from candidates who bring:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A bachelor’s degree in a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience in lab courses, research projects, or clinical settings (internships, volunteering, or academic labs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and the ability to follow structured protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and time management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear communication skills and comfort interacting with patients and team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A genuine interest in healthcare, research, or improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience as a CRC is required for some locations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2856\u0026quot; data-end=\u0026quot;2859\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2861\u0026quot; data-end=\u0026quot;2911\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;mjivf9\u0026quot; data-start=\u0026quot;2659\u0026quot; data-end=\u0026quot;2722\u0026quot;\u0026gt;Why Start or Grow Your Career in Clinical Research with Us\u0026lt;/h2\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2724\u0026quot; data-end=\u0026quot;3207\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;ei31u1\u0026quot; data-start=\u0026quot;2724\u0026quot; data-end=\u0026quot;2799\u0026quot;\u0026gt;A strong entry point into the clinical research and healthcare industry\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;15r2k4q\u0026quot; data-start=\u0026quot;2800\u0026quot; data-end=\u0026quot;2874\u0026quot;\u0026gt;Hands-on experience working with patients and clinical trial protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1scu9u3\u0026quot; data-start=\u0026quot;2875\u0026quot; data-end=\u0026quot;2949\u0026quot;\u0026gt;Opportunities to learn GCP, regulatory processes, and study operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;25y7gl\u0026quot; data-start=\u0026quot;2950\u0026quot; data-end=\u0026quot;3026\u0026quot;\u0026gt;Mentorship and training to help you build a long-term career in research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;15h47x7\u0026quot; data-start=\u0026quot;3027\u0026quot; data-end=\u0026quot;3113\u0026quot;\u0026gt;Clear pathways for growth into CRCII, III, and senior, regulatory, or leadership roles\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;ujz86f\u0026quot; data-start=\u0026quot;3114\u0026quot; data-end=\u0026quot;3207\u0026quot;\u0026gt;The chance to contribute to the development of new treatments that impact patients’ lives\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;3209\u0026quot; data-end=\u0026quot;3212\u0026quot;\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1parebi\u0026quot; data-start=\u0026quot;3214\u0026quot; data-end=\u0026quot;3251\u0026quot;\u0026gt;Ready to Start the Conversation?\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;3253\u0026quot; data-end=\u0026quot;3420\u0026quot;\u0026gt;Whether you’re an experienced coordinator or a recent graduate looking to apply your lab and academic experience in a real-world setting, we’d love to hear from you.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;3422\u0026quot; data-end=\u0026quot;3633\u0026quot;\u0026gt;Apply here to be considered for current and future Clinical Research Coordinator opportunities. Our Talent Acquisition team will reach out as roles become available that align with your background and interests.\u0026lt;/p\u0026gt;\n\u0026lt;p style=\u0026quot;text-align: left;\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$45,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$100,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004740009,"name":"Arizona - Scottsdale","location":"Scottsdale, Arizona, United States","child_ids":[],"parent_id":4004735009},{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004756009,"name":"Canada - Kelowna, BC","location":"Kelowna, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004755009,"name":"Canada - Richmond, BC","location":"Richmond, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004757009,"name":"Canada - Toronto, ON","location":"Toronto, Ontario, Canada","child_ids":[],"parent_id":4004734009},{"id":4004750009,"name":"Florida - Lake Worth","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004751009,"name":"Florida - Orlando","location":"Orlando, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009},{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009},{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009},{"id":4004745009,"name":"Michigan - Detroit","location":"Southfield, Michigan, United States","child_ids":[],"parent_id":4004734009},{"id":4004747009,"name":"Minnesota - Twin Cities","location":null,"child_ids":[],"parent_id":4004734009},{"id":4004744009,"name":"Missouri - Springfield","location":"Springfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004754009,"name":"North Carolina - Wilmington","location":"Wilmington, North Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004741009,"name":"Oregon - Portland","location":"Portland, Oregon, United States","child_ids":[],"parent_id":4004735009},{"id":4007276009,"name":"Puerto Rico - San Juan","location":"San Juan, Puerto Rico","child_ids":[],"parent_id":4004733009},{"id":4004753009,"name":"South Carolina - Myrtle Beach","location":"Myrtle Beach, South Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009},{"id":4004746009,"name":"Texas - El Paso","location":"El Paso, Texas, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4226941009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4132813009,"location":{"name":"Escondido, California"},"metadata":null,"id":4226941009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"233","title":"Clinical Research Coordinator I, II, or III","company_name":"Headlands Research","first_published":"2026-05-13T12:03:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;668\u0026quot; data-end=\u0026quot;792\u0026quot;\u0026gt;📍 Escondido, CA\u0026lt;br data-start=\u0026quot;687\u0026quot; data-end=\u0026quot;690\u0026quot;\u0026gt;🏥 AMCR Institute (a Headlands Research site)\u0026lt;br data-start=\u0026quot;748\u0026quot; data-end=\u0026quot;751\u0026quot;\u0026gt;🕒\u0026amp;nbsp;Full-time \u0026lt;strong\u0026gt;|\u0026lt;/strong\u0026gt; Onsite (no opportunities for hybrid or remote)\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;794\u0026quot; data-end=\u0026quot;876\u0026quot;\u0026gt;For experienced CRCs looking for stability, collaboration, and meaningful work\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;877\u0026quot; data-end=\u0026quot;1122\u0026quot;\u0026gt;If you’re an experienced Clinical Research Coordinator I, II, or III who values\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;943\u0026quot; data-end=\u0026quot;1054\u0026quot;\u0026gt;strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance\u0026lt;/strong\u0026gt;, Artemis Institute for Clinical Research may be the right next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;Our Escondido site is known for its \u0026lt;strong data-start=\u0026quot;1159\u0026quot; data-end=\u0026quot;1235\u0026quot;\u0026gt;depth of experience, thoughtful study execution, and team-based approach\u0026lt;/strong\u0026gt; to clinical research—particularly in metabolic studies.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1325\u0026quot; data-end=\u0026quot;1328\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1330\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1333\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;About AMCR Institute\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials. The site conducts studies focused on pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines. With a passionate and experienced team, AMCR Institute partners with sponsors and CROs to deliver meticulous research while prioritizing the care, safety, and confidentiality of every participant. By accelerating access to innovative therapies, the site makes a meaningful difference in the lives of the many affected by metabolic and immunologic conditions.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2096\u0026quot; data-end=\u0026quot;2099\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2104\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced CRCs Choose AMCR Institute\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2145\u0026quot; data-end=\u0026quot;2212\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2251\u0026quot;\u0026gt;Multi-disciplinary collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with seasoned investigators and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2303\u0026quot; data-end=\u0026quot;2346\u0026quot;\u0026gt;Strong operational support and clear SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2349\u0026quot; data-end=\u0026quot;2420\u0026quot;\u0026gt;Exposure to complex, meaningful studies—not just high-volume turnover\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2487\u0026quot; data-end=\u0026quot;2555\u0026quot;\u0026gt;Backing of a growing research network with resources and stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for CRCs who enjoy\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2595\u0026quot; data-end=\u0026quot;2619\u0026quot;\u0026gt;owning their studies\u0026lt;/strong\u0026gt;, working with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2634\u0026quot; data-end=\u0026quot;2653\u0026quot;\u0026gt;competent teams\u0026lt;/strong\u0026gt;, and being trusted to execute with precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Provide the highest level of care for study patients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Deliver excellent customer service to pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation through close-out\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention activities\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Ensure timely EDC data entry and resolution of queries\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Report and follow up on AEs, SAEs, and protocol deviations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Collaborate with investigators, sponsors/CROs, labs, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain regulatory documentation and ensure training compliance for amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;High school diploma or GED required\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Experience with EDC, IVRS, and clinical research platforms\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong organizational skills with the ability to manage multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Clear, professional verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Comfortable working onsite in a collaborative, clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4906\u0026quot; data-end=\u0026quot;4909\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4911\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4914\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;CRCs who want\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4959\u0026quot; data-end=\u0026quot;5001\u0026quot;\u0026gt;structure, support, and accountability\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those interested in taking the next step in managing people\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5030\u0026quot; data-end=\u0026quot;5053\u0026quot;\u0026gt;teamwork over silos\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Coordinators who care about data quality, patient experience, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those ready to grow within a stable, well-established research site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5210\u0026quot; data-end=\u0026quot;5213\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;📬\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5218\u0026quot; data-end=\u0026quot;5233\u0026quot;\u0026gt;Apply today\u0026lt;/strong\u0026gt;\u0026amp;nbsp;if you’re looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$72,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$85,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4226823009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4132751009,"location":{"name":"Portland, Oregon"},"metadata":null,"id":4226823009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"232","title":"Clinical Research Coordinator I or II","company_name":"Headlands Research","first_published":"2026-04-22T09:37:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;668\u0026quot; data-end=\u0026quot;792\u0026quot;\u0026gt;📍 Portland, OR\u0026lt;br data-start=\u0026quot;687\u0026quot; data-end=\u0026quot;690\u0026quot;\u0026gt;🏥 Summit Research Network\u0026lt;br data-start=\u0026quot;748\u0026quot; data-end=\u0026quot;751\u0026quot;\u0026gt;🕒 Full-time \u0026lt;strong\u0026gt;|\u0026lt;/strong\u0026gt; Onsite (no opportunities for hybrid or remote)\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;794\u0026quot; data-end=\u0026quot;876\u0026quot;\u0026gt;For experienced CRCs looking for stability, collaboration, and meaningful work\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;877\u0026quot; data-end=\u0026quot;1122\u0026quot;\u0026gt;If you’re an experienced Clinical Research Coordinator who values\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;943\u0026quot; data-end=\u0026quot;1054\u0026quot;\u0026gt;strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance\u0026lt;/strong\u0026gt;, Summit Research Network may be the right next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;Our Portland site is known for its \u0026lt;strong data-start=\u0026quot;1159\u0026quot; data-end=\u0026quot;1235\u0026quot;\u0026gt;depth of experience, thoughtful study execution, and team-based approach\u0026lt;/strong\u0026gt; to clinical research—particularly in memory studies.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1325\u0026quot; data-end=\u0026quot;1328\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1330\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1333\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;About Summit Research Network\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;Since 1976, Summit Research Network has worked in cooperation with pharmaceutical companies to develop new medical treatments for various of conditions by conducting 500+ clinical trials. With decades of experience, Summit Research Network provides the most advanced clinical research, including our Memory Health Center, to help develop better treatments and better future health for individuals with psychiatric, dementia, age related memory issues and many other health conditions.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2096\u0026quot; data-end=\u0026quot;2099\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2104\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced CRCs Choose Summit\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2145\u0026quot; data-end=\u0026quot;2212\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2251\u0026quot;\u0026gt;Multi-disciplinary collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with seasoned investigators and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2303\u0026quot; data-end=\u0026quot;2346\u0026quot;\u0026gt;Strong operational support and clear SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2349\u0026quot; data-end=\u0026quot;2420\u0026quot;\u0026gt;Exposure to complex, meaningful studies—not just high-volume turnover\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2487\u0026quot; data-end=\u0026quot;2555\u0026quot;\u0026gt;Backing of a growing research network with resources and stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for CRCs who enjoy\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2595\u0026quot; data-end=\u0026quot;2619\u0026quot;\u0026gt;owning their studies\u0026lt;/strong\u0026gt;, working with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2634\u0026quot; data-end=\u0026quot;2653\u0026quot;\u0026gt;competent teams\u0026lt;/strong\u0026gt;, and being trusted to execute with precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Provide the highest level of care for study patients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Deliver excellent customer service to pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation through close-out\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention activities\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Ensure timely EDC data entry and resolution of queries\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Report and follow up on AEs, SAEs, and protocol deviations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Collaborate with investigators, sponsors/CROs, labs, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain regulatory documentation and ensure training compliance for amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Experience with EDC, IVRS, and clinical research platforms\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong organizational skills with the ability to manage multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Clear, professional verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Comfortable working onsite in a collaborative, clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4906\u0026quot; data-end=\u0026quot;4909\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4911\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4914\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;CRCs who want\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4959\u0026quot; data-end=\u0026quot;5001\u0026quot;\u0026gt;structure, support, and accountability\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those interested in taking the next step in managing people\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5030\u0026quot; data-end=\u0026quot;5053\u0026quot;\u0026gt;teamwork over silos\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Coordinators who care about data quality, patient experience, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those ready to grow within a stable, well-established research site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5210\u0026quot; data-end=\u0026quot;5213\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;📬\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5218\u0026quot; data-end=\u0026quot;5233\u0026quot;\u0026gt;Apply today\u0026lt;/strong\u0026gt; if you’re looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004741009,"name":"Oregon - Portland","location":"Portland, Oregon, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4266539009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4155822009,"location":{"name":"Escondido, California"},"metadata":null,"id":4266539009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"268","title":"Clinical Research Manager","company_name":"Headlands Research","first_published":"2026-06-03T16:34:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Research Manager combines the responsibilities of supporting the coordination of clinical trials along with leading and overseeing the research department. \u0026amp;nbsp; This role requires strong leadership skills to guide and mentor staff, provide strategic direction, manage resources, and foster a collaborative environment to achieve research objectives. \u0026amp;nbsp;The Clinical Research Manager ensures that all studies are conducted in compliance with regulatory requirements and protocols, and that data is accurately collected and reported.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Escondido, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Clinical Trial Management:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee, coordinate, and manage multiple clinical trials from initiation to completion. This may include coordinating trials and/or managing the clinical trials team of CRCs and RAs who coordinate the trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with research protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recruit, enroll, and manage study participants throughout the entire study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain informed consent from participants and ensure their understanding of the study, collect data using Good Documentation Practices, , maintain accurate and up-to-date records of study activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate with study sponsors, regulatory bodies, and other stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and submit regulatory documents as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure proper storage and handling of study specimens and investigational products.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leadership and Mentorship:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and mentor junior research staff, providing guidance and support until mastery in needed skills is demonstrated.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a collaborative and productive work environment that encourages continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead regular team meetings to discuss status of current projects, plan for future projects, provide updates on new company initiatives, seek feedback regarding team barriers, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage local team to meet/exceed quality and performance metrics, report key performance indicators to leadership team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a Culture Champion to support our mission and values, ensure team is compliant with SOPs and all industry standards.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic Planning and Growth:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement strategic plans for clinical research projects, allocate studies to the team based on bandwidth and teammate skillset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive the growth and development of the clinical research program by identifying areas for improvement and innovation while staying informed of industry advancements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify/anticipate risks (strategically, operational, financial, regulatory, and reputational) that could hinder achievement of business goals.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conflict Resolution:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Address and resolve conflicts within the research team and with external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mediate disputes and facilitate effective communication.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement strategies to prevent and manage conflicts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in a scientific, health-related, or business administration field. Advanced degree (e.g., Master\u0026#39;s, PhD) is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of experience in clinical research, with at least 2 years in a senior or leadership role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of project management principles and methodologies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and time-management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and ability to work independently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving and critical thinking abilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle multiple tasks and prioritize effectively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong ethical standards and professionalism.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven leadership skills and experience in mentoring staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to inspire and motivate a team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking and planning abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Growth mindset and a commitment to continuous improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong conflict resolution and mediation skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage and resolve disputes effectively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Electronic Data Capture (EDC) systems and clinical trial management software.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$100,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$105,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005116009,"name":"Operations \u0026 Site Leadership","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4138505009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4091071009,"location":{"name":"Plymouth, Massachusetts"},"metadata":null,"id":4138505009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"158","title":"Clinical Research Nurse","company_name":"Headlands Research","first_published":"2026-02-24T09:42:34-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced Clinical Research Nurse to help us grow our Headlands Research Eastern Massachusetts site located in Plymouth, MA. The Clinical Research Nurse is a flexible and essential member of the research team, skilled in performing a wide range of duties that support the site’s operational and clinical objectives. Key responsibilities include preparing and administering therapies, including IV infusions, monitoring study participants, and thoroughly documenting all clinical activities. This role also encompasses conducting intake procedures and performing cognitive assessments. The Clinical Research Nurse is expected to maintain clear and effective communication with the clinical trial team to promote participant safety, protocol compliance, and overall satisfaction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as a research nurse and experience with infusions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Plymouth, MA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Monday - Friday, 8:00am-4:00pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Conducts patient health assessments and medication administration\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtains IV access through peripheral IV initiation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepares and administers a variety of specialized intravenous or injectable pharmacological treatments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides study participant care by utilizing the skills of observation, assessment, nursing diagnosis, counseling, health teaching, and reporting any adverse events to immediate supervisor or required stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs routine nursing duties in accordance with company policies and procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs specialized nursing procedures for which recognized training and current competency have been demonstrated and completed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Observes and documents study participant conditions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Acts as a resource to other nurses by providing support and direction as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understands and implements infection prevention practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in ongoing internal and/or external continuing education activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adheres to Headlands EMA policies and procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in quality activities and continuous improvement initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in proactive Health \u0026amp;amp; Safety activities while performing all duties. Is responsible to notify immediate Supervisor of any Health \u0026amp;amp; Safety risks or concerns.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains confidentiality of client and corporate information.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Completes other tasks as requested.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains knowledge of study protocols, including inclusion and exclusion criteria for each study protocol in order to assist with screening potential study participants for participation as part of our recruitment process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contact potential study participants who have requested information on our enrolling studies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license as a Registered Nurse (RN) in the state of Massachusetts required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience with providing multiple daily infusions required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Neurology experience highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Graduation from an accredited nursing education program with a Bachelor of Science in Nursing (BSN) degree or equivalent preferred, but not required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional peripheral IV initiation skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional clinical assessment skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to manage relationships with exceptional customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional interpersonal skills and ability to handle difficult situations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to work independently and as part of an interdisciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to perform and prioritize multiple functions and tasks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to read and interpret technical instructions related to clinical care\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005108009,"name":"Clinical: Nurses \u0026 Infusionists","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4106707009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4059856009,"location":{"name":"Plymouth, MA"},"metadata":null,"id":4106707009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"110","title":"Clinical Research Site Director","company_name":"Headlands Research","first_published":"2026-01-16T10:09:00-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Site Director – Transformational Clinical Research Leader\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div id=\u0026quot;x_prosemirror-editor-container\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;The Opportunity\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Are you a seasoned clinical research leader ready to\u0026amp;nbsp;\u0026lt;strong\u0026gt;turn challenge into momentum\u0026lt;/strong\u0026gt;? We are seeking a bold, hands-on\u0026amp;nbsp;\u0026lt;strong\u0026gt;Site Director\u0026lt;/strong\u0026gt;\u0026amp;nbsp;to step into a clinical research site with untapped potential and lead its transformation into a high-performing, patient-centered operation.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;This is not a maintenance role—it’s a\u0026amp;nbsp;\u0026lt;strong\u0026gt;build, elevate, and lead\u0026lt;/strong\u0026gt;\u0026amp;nbsp;opportunity. You will have the autonomy, visibility, and support to implement best-in-class operational processes, mentor and inspire your team, and directly impact enrollment performance, data quality, and financial outcomes. If you thrive in environments where your leadership truly matters, this role offers the chance to leave a lasting mark.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;hr width=\u0026quot;100%\u0026quot;\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;What You’ll Do\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;As Site Director, you will serve as the operational and cultural heartbeat of the site—balancing strategy with execution and leadership with accountability.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Lead \u0026amp;amp; Inspire\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Coach, mentor, and develop site staff to reach their highest potential and operate as a cohesive, high-performing team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Establish a culture of ownership, accountability, and continuous improvement\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Champion patient experience, retention strategies, and enrollment excellence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Drive Performance\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Own site-level KPIs, including enrollment targets, financial performance, and quality metrics\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Implement and optimize operational systems and workflows to improve efficiency and outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Collaborate with the Business Development team\u0026amp;nbsp;and Sponsors/CROs\u0026amp;nbsp;to ensure the site has a consistent pipeline of awarded studies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Own the Financials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Oversee financial performance across trials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Maintain accountability for invoicing\u0026amp;nbsp;accuracy\u0026amp;nbsp;and financial forecasting\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;hr width=\u0026quot;100%\u0026quot;\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Who You Are\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;You’re a proven clinical research professional with leadership instincts, financial acumen, and the resilience to lead through change. You approach \u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;evolving operations with confidence and optimism, recognizing their potential to become success stories under strong leadership.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Bachelor’s degree required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;3+ years of experience in clinical trials (as a primary study coordinator, project coordinator, or similar role)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;ul type=\u0026quot;circle\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Previous experience at the site-level required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;3+ years of people management experience within the healthcare industry required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;ul type=\u0026quot;circle\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Experience with change management techniques highly valued\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Strong understanding of clinical trial operations and site-level financials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;What Sets You Apart\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Highly detail-oriented with exceptional organizational skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Strong critical thinker who can prioritize, problem-solve, and execute under pressure\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Comfortable managing multiple priorities without losing sight of the big picture\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Tech-savvy with strong computer and reporting skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Clear, confident communicator with the ability to build trust across teams and external partners\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Customer- and patient-focused mindset\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;hr width=\u0026quot;100%\u0026quot;\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Why This Role Matters\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;This is a rare opportunity to\u0026amp;nbsp;\u0026lt;strong\u0026gt;step into a leadership role where your impact will be visible, measurable, and meaningful\u0026lt;/strong\u0026gt;. You’ll have the chance to stabilize, grow, and ultimately redefine what success looks like for a clinical research site—and for your own career.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;If you’re ready to lead with purpose, drive results, and build something better, we’d love to meet you.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005116009,"name":"Operations \u0026 Site Leadership","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4266556009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4155831009,"location":{"name":"Riverside, California"},"metadata":null,"id":4266556009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"269","title":"Clinical Research Site Manager","company_name":"Headlands Research","first_published":"2026-06-03T16:32:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Site Manager performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of the site operations.\u0026amp;nbsp;The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Riverside, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strategic and Operational Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Evaluates overall performance of the Site and recommends and implements processes and plans for improvement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for maintaining a site calendar to ensure adequate enrollment for studies and coordination of employee PTO.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Staff Development and Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Fosters a culture of excellence, teamwork, and innovation among site staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hires, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registered Nurses, support personnel, etc.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supervises performance of other Clinical Research Coordinators, Research Assistants, and support staff at the Site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Quality Assurance \u0026amp;amp; Compliance\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintains up-to-date knowledge of all relevant regulatory guidelines and requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures the site’s compliance with FDA, ICH, and local regulatory agency regulations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical Research Coordination\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In addition to assuming management responsibilities as a Site Manager, this individual performs the duties of a Clinical Research Coordinator\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Protects the rights, safety, and welfare of human subjects, follows Good Clinical Practice, and works cooperatively with others\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitors study activities to ensure compliance with study protocols, with site policies, and with applicable federal, state, and local regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the planning, initiation, and execution of clinical trials at the site\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manages and optimizes patient recruitment and retention efforts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other healthcare professionals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Addresses any patient concerns or issues promptly and professionally\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Documentation and Reporting\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Documents findings and events in the CTMS platform and in other binders and platforms as directed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performs other duties as assigned, including duties routinely performed by the Company’s Research Assistants\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2-4 clinical research trials, simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in FDA regulations governing clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong supervisory skills to lead research staff effectively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to collect and manage research data accurately\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with documentation review processes in clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of medical terminology relevant to clinical trials management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;IATA (dangerous goods handling)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;GCP (Good Clinical Practice)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills with all members of the team.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capability to perform phlebotomy procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CCRC or CCRP certified\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$100,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$105,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005116009,"name":"Operations \u0026 Site Leadership","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4193948009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4114164009,"location":{"name":"Remote"},"metadata":null,"id":4193948009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"196","title":"Clinical Trials Site Director – Multiple Locations Nationwide","company_name":"Headlands Research","first_published":"2026-04-23T11:44:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;588\u0026quot;\u0026gt;About the Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We’re always interested in connecting with experienced clinical research leaders who are passionate about building high-performing sites and advancing patient access to clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This general interest posting is designed for Site Directors who may not see a current opening that aligns with their location—but who would like to be considered for future leadership opportunities across our growing network of clinical research sites nationwide.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Our Site Directors play a critical role in driving site performance, leading cross-functional teams, and ensuring the successful execution of clinical trials in a compliant, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1244\u0026quot; data-end=\u0026quot;1247\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1249\u0026quot; data-end=\u0026quot;1294\u0026quot;\u0026gt;Our Process\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1339\u0026quot; data-end=\u0026quot;1755\u0026quot;\u0026gt;When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;1448\u0026quot; data-end=\u0026quot;1496\u0026quot;\u0026gt;current and upcoming opportunities\u0026lt;/strong\u0026gt;. As new roles open, we proactively match candidates based on \u0026lt;strong data-start=\u0026quot;1558\u0026quot; data-end=\u0026quot;1644\u0026quot;\u0026gt;location preference, specialty, prior research experience, and leadership interest\u0026lt;/strong\u0026gt;. If a role aligns with your background and goals, a recruiter will reach out directly to begin a conversation.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1757\u0026quot; data-end=\u0026quot;1760\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1762\u0026quot; data-end=\u0026quot;1810\u0026quot;\u0026gt;What Site Director Roles Look Like at Our Company\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;Site Directors are responsible for the overall performance of a clinical research site, including operational execution, team leadership, patient recruitment, and financial outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role partners closely with investigators, sponsors, and internal teams to ensure studies are delivered on time, within budget, and in full compliance with regulatory requirements. Site Directors also play a key role in developing site teams, improving processes, and scaling operations as we continue to grow.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2351\u0026quot; data-end=\u0026quot;2354\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2356\u0026quot; data-end=\u0026quot;2380\u0026quot;\u0026gt;Who We’re Looking For\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We welcome interest from professionals who bring:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience leading operations within a clinical research site or healthcare environment practice\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong leadership skills with the ability to build, develop, and retain high-performing teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A track record of driving performance, including patient recruitment, study execution, and financial outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operational and financial acumen, with experience managing budgets and site-level metrics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A commitment to quality, compliance, and patient safety\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The ability to collaborate effectively with physicians, sponsors, and cross-functional partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in clinical research is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2856\u0026quot; data-end=\u0026quot;2859\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2861\u0026quot; data-end=\u0026quot;2911\u0026quot;\u0026gt;Why Join our Network\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Opportunity to lead and shape the performance of a clinical research site\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct impact on expanding patient access to innovative therapies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support from centralized infrastructure, including regulatory, recruitment, and business development teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;The ability to grow within a rapidly expanding, multi-site organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven environment focused on quality, patients, and innovation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;3263\u0026quot; data-end=\u0026quot;3266\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;3268\u0026quot; data-end=\u0026quot;3303\u0026quot;\u0026gt;Ready to Start the Conversation?\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;3305\u0026quot; data-end=\u0026quot;3538\u0026quot;\u0026gt;If you’re interested in learning more about Site Director opportunities within clinical research—now or in the future—we invite you to apply here. Our Talent Acquisition team looks forward to connecting when the right opportunity arises.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005116009,"name":"Operations \u0026 Site Leadership","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4173337009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4100255009,"location":{"name":"Remote"},"metadata":null,"id":4173337009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"172","title":"Director of Strategic Partnerships","company_name":"Headlands Research","first_published":"2026-03-05T14:23:34-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director of Strategic Partnerships is a strategic leadership role responsible for identifying, developing, and managing high-impact collaborations between our research network and biotechnology and pharmaceutical companies. You will serve as the primary bridge between external innovators and our clinical operations teams, driving revenue growth and ensuring our sites remain the \u0026quot;partners of choice\u0026quot; for cutting-edge clinical trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Strategic Business Development:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Biotech account management on pre-identified accounts. Foster and maintain relationships with key assigned accounts. Identify and evaluate potential biotech partners whose pipelines align with our site group’s therapeutic expertise utilizing our internal tools and existing relationships. Strategic and highly organized with a clearly defined path to accomplish sales goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Relationship Management:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Act as the\u0026amp;nbsp;Primary Clinical Site Liaison\u0026amp;nbsp;to nurture long-term, senior-level relationships with Sponsors and more particularly the assigned account Sponsors provided. Established senior level industry partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Partnership Lifecycle Oversight:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Lead end-to-end partnership cycles, from initial prospecting and capability presentations to award and partnership maintenance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Operational Alignment:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Partner with site directors and clinical leads to ensure proposed trials are operationally feasible and aligned with site resources.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Market Intelligence:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Stay informed on emerging therapeutic trends, AI-driven research tools, and the competitive landscape to refine our value proposition.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Education: \u0026lt;/strong\u0026gt;Bachelor’s degree in a scientific or business discipline required; an advanced degree (PhD, PharmD, or MBA) is preferred but not required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt; 5-10 years of experience in site operations, business development, or alliance management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Technical Knowledge: \u0026lt;/strong\u0026gt;Deep understanding site operations and pharma relationships/drug development timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Communication: \u0026lt;/strong\u0026gt;Exceptional presentation skills, with the ability to translate complex site capabilities and patient access into clear business value. Ability to communicate clearly and effectively both internally and externally.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Project Management: \u0026lt;/strong\u0026gt;Proven ability to manage multiple high-impact collaborations simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Fully Remote, travel required\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Chief Business Development Officer\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005117009,"name":"Business Development","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4247659009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4144697009,"location":{"name":"Kelowna, British Columbia"},"metadata":null,"id":4247659009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"255","title":"Laboratory Technician / Phlebotomist","company_name":"Headlands Research","first_published":"2026-05-15T09:24:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p data-start=\u0026quot;481\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;📍 \u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Kelowna, BC\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;500\u0026quot; data-end=\u0026quot;503\u0026quot;\u0026gt;🏥 \u0026lt;strong data-start=\u0026quot;506\u0026quot; data-end=\u0026quot;558\u0026quot;\u0026gt;Okanagan Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;558\u0026quot; data-end=\u0026quot;561\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Full-Time | Monday through Friday, 8am - 4:30pm\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;481\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Pay: CAD $52,000 - $58,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;622\u0026quot; data-end=\u0026quot;677\u0026quot;\u0026gt;\u0026lt;em\u0026gt;Looking for more than just high-volume blood draws?\u0026lt;/em\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;678\u0026quot; data-end=\u0026quot;887\u0026quot;\u0026gt;If you’re a phlebotomist or lab technician who takes pride in precision, patient care, and doing things the\u0026amp;nbsp;\u0026lt;em data-start=\u0026quot;799\u0026quot; data-end=\u0026quot;806\u0026quot;\u0026gt;right\u0026lt;/em\u0026gt;\u0026amp;nbsp;way—not just the fast way—clinical research may be the next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;889\u0026quot; data-end=\u0026quot;1124\u0026quot;\u0026gt;At \u0026lt;strong data-start=\u0026quot;892\u0026quot; data-end=\u0026quot;919\u0026quot;\u0026gt;Okanagan Clinical Trials\u0026lt;/strong\u0026gt;, our lab professionals work in a\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;953\u0026quot; data-end=\u0026quot;1005\u0026quot;\u0026gt;structured, calm, and purpose-driven environment\u0026lt;/strong\u0026gt;, supporting clinical trials that help advance new treatments for psychiatric, dementia, and memory-related conditions.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;889\u0026quot; data-end=\u0026quot;1124\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1126\u0026quot; data-end=\u0026quot;1129\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1131\u0026quot; data-end=\u0026quot;1184\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1134\u0026quot; data-end=\u0026quot;1184\u0026quot;\u0026gt;Why Lab Professionals Choose Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1187\u0026quot; data-end=\u0026quot;1266\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1187\u0026quot; data-end=\u0026quot;1219\u0026quot;\u0026gt;Predictable weekday schedule\u0026lt;/strong\u0026gt;\u0026amp;nbsp;(no nights, no weekends, no emergency draws)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1269\u0026quot; data-end=\u0026quot;1340\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1269\u0026quot; data-end=\u0026quot;1294\u0026quot;\u0026gt;More time and control\u0026lt;/strong\u0026gt;\u0026amp;nbsp;during patient visits and specimen handling\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1343\u0026quot; data-end=\u0026quot;1431\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1343\u0026quot; data-end=\u0026quot;1367\u0026quot;\u0026gt;Specialized lab work\u0026lt;/strong\u0026gt;\u0026amp;nbsp;beyond routine phlebotomy (processing, PK handling, shipping)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1434\u0026quot; data-end=\u0026quot;1497\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1434\u0026quot; data-end=\u0026quot;1466\u0026quot;\u0026gt;Smaller, collaborative teams\u0026lt;/strong\u0026gt;\u0026amp;nbsp;where your role is respected\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1500\u0026quot; data-end=\u0026quot;1578\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1500\u0026quot; data-end=\u0026quot;1522\u0026quot;\u0026gt;Meaningful purpose\u0026lt;/strong\u0026gt;—your work directly supports future medical treatments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;1652\u0026quot; data-end=\u0026quot;1826\u0026quot;\u0026gt;This role is ideal for lab professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;1703\u0026quot; data-end=\u0026quot;1746\u0026quot;\u0026gt;accuracy, organization, and consistency\u0026lt;/strong\u0026gt;, and who want to grow their skills beyond traditional lab or hospital settings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2511\u0026quot; data-end=\u0026quot;2514\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2516\u0026quot; data-end=\u0026quot;2531\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2519\u0026quot; data-end=\u0026quot;2531\u0026quot;\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;2532\u0026quot; data-end=\u0026quot;2801\u0026quot;\u0026gt;The Phlebotomist/Lab Tech is a key member of the clinical research team, supporting studies through\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2647\u0026quot; data-end=\u0026quot;2711\u0026quot;\u0026gt;specimen collection, processing, documentation, and shipment\u0026lt;/strong\u0026gt;\u0026amp;nbsp;in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2803\u0026quot; data-end=\u0026quot;2987\u0026quot;\u0026gt;You’ll work in a controlled clinical research environment with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2866\u0026quot; data-end=\u0026quot;2938\u0026quot;\u0026gt;scheduled visits, detailed protocols, and strong operational support\u0026lt;/strong\u0026gt;, allowing you to focus on quality and precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2803\u0026quot; data-end=\u0026quot;2987\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4883\u0026quot; data-end=\u0026quot;4886\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4888\u0026quot; data-end=\u0026quot;4919\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4891\u0026quot; data-end=\u0026quot;4919\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4922\u0026quot; data-end=\u0026quot;4976\u0026quot;\u0026gt;Lab professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4950\u0026quot; data-end=\u0026quot;4974\u0026quot;\u0026gt;precision over speed\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4979\u0026quot; data-end=\u0026quot;5037\u0026quot;\u0026gt;Phlebotomists looking for\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5005\u0026quot; data-end=\u0026quot;5035\u0026quot;\u0026gt;predictability and balance\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5040\u0026quot; data-end=\u0026quot;5102\u0026quot;\u0026gt;Candidates curious about clinical research and career growth\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5105\u0026quot; data-end=\u0026quot;5181\u0026quot;\u0026gt;Team players who take pride in quality, compliance, and patient experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5183\u0026quot; data-end=\u0026quot;5186\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare lab kits for each subject based on study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ship biological specimens following IATA guidelines and protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain specimen logs, shipping records, temperature logs, and other documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean and sanitize lab equipment and work areas daily.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to and resolve electronic data queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify accuracy and completeness of data entries and study documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in quality control and assurance initiatives to ensure regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and maintain inventory of lab kits and supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Order dry ice and other lab necessities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Destroy expired kits and log per protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation of study-specific training materials and lab manuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with study coordinators and medical staff to meet visit protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May assist with infusion monitoring under clinician supervision.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Must be certified in phlebotomy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous healthcare experience preferred; direct patient care experience a huge bonus!\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in clinical research is a huge plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be comfortable with performing Research Assistant tasks when the lab is slow.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle potentially hazardous materials safely.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, time management, and multitasking skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication; strong interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and as part of a cross-functional team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Customer-service mindset and high level of professionalism.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Okanagan Clinical Trials is a Headlands Research site. Our clinic specializes in the execution of research studies that hope to advance treatments for many indications including Alzheimer’s disease, migraine, COPD, stress urinary incontinence, celiac disease, diabetes, and more.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005110009,"name":"Clinical: Laboratory","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004756009,"name":"Canada - Kelowna, BC","location":"Kelowna, British Columbia, Canada","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4254956009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4149060009,"location":{"name":"Baltimore, Maryland"},"metadata":null,"id":4254956009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"259","title":"Medical Assistant - Research Assistant","company_name":"Headlands Research","first_published":"2026-05-21T11:11:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;167\u0026quot; data-end=\u0026quot;247\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-exfc11cw_A\u0026quot;\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong\u0026gt;Pikesville, MD\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-qFsrSOZK5Z\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong\u0026gt;PharmaSite Research\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-Ez0pTXSu9i\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong\u0026gt;Full-Time | Monday through Friday | 9:00am - 5:00pm\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;Launch Your Career in Healthcare \u0026amp;amp; Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;268\u0026quot; data-end=\u0026quot;528\u0026quot;\u0026gt;Are you a recent graduate looking to gain hands-on experience in healthcare or clinical research? This is an exciting opportunity to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;530\u0026quot; data-end=\u0026quot;935\u0026quot;\u0026gt;As a\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;535\u0026quot; data-end=\u0026quot;566\u0026quot;\u0026gt;Clinical Research Assistant\u0026lt;/strong\u0026gt;, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you\u0026#39;re planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;299\u0026quot; data-end=\u0026quot;612\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;951\u0026quot; data-end=\u0026quot;954\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;xti9y5\u0026quot; data-start=\u0026quot;956\u0026quot; data-end=\u0026quot;976\u0026quot;\u0026gt;Responsibilities:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Study Preparation\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participant Care and Interaction\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with participant stipend tracking and processing.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Laboratory and Specimen Handling\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and file weekly temperature reports for laboratory systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Entry and Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administrative and General Support\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings, study teleconferences, and trainings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with onsite or remote clinical research monitor visits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1487\u0026quot; data-end=\u0026quot;1490\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1f5kc01\u0026quot; data-start=\u0026quot;1492\u0026quot; data-end=\u0026quot;1524\u0026quot;\u0026gt;What Makes You a Great Fit\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and ability to follow step-by-step procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work efficiently in a fast-paced environment with changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills and a professional, patient-focused demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable interacting with a diverse patient population\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, dependable, and eager to learn new skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance multiple tasks and priorities throughout the day\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional, reliable, and eager to learn\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2035\u0026quot; data-end=\u0026quot;2038\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Requirements:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2393\u0026quot;\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience as or certification/license as a CNA, Medical Assistant, Phlebotomist, or other direct-patient-care healthcare role required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with medical terminology and laboratory procedures helpful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, with the ability to collect, compile, and analyze patient data accurately.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, communication (verbal and written), and customer service skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Easily able to learn new computer or website applications (i.e. Electronic Medical Records, Clinial Trial Management Systems, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to prioritize tasks, meet deadlines, and adapt to a fast-paced work environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving skills with a proactive and solution-oriented approach.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills with the proven ability to prioritize tasks and meet strict deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xrynm\u0026quot; data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2100\u0026quot;\u0026gt;Phlebotomy training and experience heavily preferred; willingness to become fully trained required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2395\u0026quot; data-end=\u0026quot;2398\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;iyhmpw\u0026quot; data-start=\u0026quot;2400\u0026quot; data-end=\u0026quot;2441\u0026quot;\u0026gt;Why This Role is a Great First Step\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;wylw1b\u0026quot; data-start=\u0026quot;3300\u0026quot; data-end=\u0026quot;3381\u0026quot;\u0026gt;Gain hands-on experience working directly with patients in a clinical setting\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;16gzdnb\u0026quot; data-start=\u0026quot;3382\u0026quot; data-end=\u0026quot;3458\u0026quot;\u0026gt;Learn the fundamentals of clinical research and how trials are conducted\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1o8ku67\u0026quot; data-start=\u0026quot;3459\u0026quot; data-end=\u0026quot;3542\u0026quot;\u0026gt;Build transferable skills for careers in healthcare, research, or biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;4waw5a\u0026quot; data-start=\u0026quot;3543\u0026quot; data-end=\u0026quot;3623\u0026quot;\u0026gt;Work alongside experienced professionals who provide training and mentorship\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1on929o\u0026quot; data-start=\u0026quot;3624\u0026quot; data-end=\u0026quot;3726\u0026quot;\u0026gt;Create a strong foundation for advancement into roles like Clinical Research Coordinator or beyond\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;uvrqhh\u0026quot; data-start=\u0026quot;3727\u0026quot; data-end=\u0026quot;3813\u0026quot;\u0026gt;Make a meaningful impact by helping bring new treatments and therapies to patients\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2768\u0026quot; data-end=\u0026quot;2771\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2773\u0026quot; data-end=\u0026quot;2928\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;If you\u0026#39;re looking to turn your academic experience into a meaningful, patient-focused career, this is a powerful place to start.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4243180009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4141749009,"location":{"name":"Rolling Hills Estates, California"},"metadata":null,"id":4243180009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"248","title":"Medical Front Desk Receptionist","company_name":"Headlands Research","first_published":"2026-05-13T16:21:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Rolling Hills Estates, CA | 🏥 Site Name: Peninsula Research Associates | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;💼 The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a \u0026lt;strong\u0026gt;Medical Front Desk Receptionist\u0026lt;/strong\u0026gt; for our clinical research site Peninsula Research Associates located in Rolling Hills Estates, CA. This pivotal role will involve managing the front desk operations and supporting the administrative tasks for the site. The ideal candidate will demonstrate strong organizational and management skills, high proficiency in technology/computer applications, and a commitment to providing excellent customer service.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 5:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026lt;/strong\u0026gt; $20-23/hr *Dependent upon relevant experience, certification, and education.\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Rolling Hills Estates/Palos Verdes, CA (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Friendly and Collaborative Culture:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Be part of a dynamic team that values collaboration and growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Professional Growth:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Opportunities for advancement in a rapidly growing organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Comprehensive Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Enjoy a range of medical and dental plans, vision coverage, 401(k) with company match, paid holidays, paid time off, and more.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Greet and assist patients in a friendly and professional manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage phone calls and schedule appointments efficiently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure the reception area is clean, organized, and welcoming.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collect patient information and maintain accurate records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with clinical staff to support operational needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle various administrative tasks as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage office supplies and equipment to ensure operational compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with facility-related expenses to ensure budget adherence.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent; certification in medical office administration is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience scheduling customer/patient appointments and handling customer/patient phone calls required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within a healthcare environment is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual in English and Spanish preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong computer skills with the ability to learn new software systems quickly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication (verbal and written) and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple tasks simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment to delivering exceptional customer service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reliable and trustworthy.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$20\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$23 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005112009,"name":"Office Support","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4226811009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4132746009,"location":{"name":"Plymouth, Massachusetts"},"metadata":null,"id":4226811009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"231","title":"Medical Receptionist","company_name":"Headlands Research","first_published":"2026-04-20T14:49:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;The Role\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Headlands Research - Eastern Massachusetts is seeking a full-time customer service-focused medical receptionist responsible for interacting with both clinic and study patients in a healthcare setting and managing administrative tasks for the clinical team. Duties include greeting patients and family via phone and in person, explaining intake forms to new patients, scheduling clinic appointments.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Administrative Assistant plays a vital role as the first point of contact for patients, visitors, and vendors in a clinical research or medical office environment. This individual ensures smooth front-office operations by managing patient flow, handling administrative tasks, and supporting the clinical team. The ideal candidate is professional, detail-oriented, and customer-service focused, with the ability to manage multiple responsibilities in a fast-paced healthcare setting.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Interacts in a professional manner at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conducts check-out, scheduling appointments for patients in the clinic\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for ordering labs tests and imaging and out of office procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain prior authorization as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;EEG scheduling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Answers telephones, takes detailed and accurate messages, and ensures messages are directed appropriately\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide intake paperwork (demographics, medical history list, medication list, surgeries)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor voice mail box and ensure messages are directed appropriately\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor faxes and ensure they are directed appropriately\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate the ordering of prescription and refills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Full Knowledge of front desk check in for back up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other tasks as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience working in a clinical environment with direct patient interaction required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent education required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical trials knowledge or experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional customer service skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive and professional attitude\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of medical terminology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in operating phones, personal computers, software and other basic IT systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate with employees, patients and other individuals in a professional and courteous manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrates high level of attention to ensure accuracy of reports and data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outstanding verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office Suite products including Excel, Word and Outlook\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable of working independently with minimal supervision and as part of a team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005112009,"name":"Office Support","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4204302009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4119300009,"location":{"name":"Chesterfield, Missouri"},"metadata":null,"id":4204302009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"207","title":"Nurse Practitioner - Clinical Research","company_name":"Headlands Research","first_published":"2026-03-31T15:14:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us - it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced Nurse Practitioner or Physician Assistant to help us grow our clinical research site located in the Greater St. Louis Area. You will help the site conduct clinical research trials involving gastroenterology, neurology, vaccines, and general internal medicine.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Professionals (CRP) is a dedicated research center that provides a network of providers who work collaboratively in conducting clinical research trials. The site’s team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time Regular Employee\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as an Investigator in clinical research.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Chesterfield, MO (no opportunities for remote or hybrid)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am-5:00pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety and welfare of each study subject\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have in-depth knowledge of all research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct medical history interviews and physical examinations throughout the subject’s study participation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review EKG’s and lab results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical care as needed during a subject’s participation in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide home based on-call availability per standard policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend Investigator Meetings on behalf of Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent professional communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Friendly and outgoing demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must demonstrate a passion for direct patient interaction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a licensed family or non-acute adult nurse practitioner or physician assistant treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an NP or PA in the state of Missouri required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within the clinical research industry highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4121279009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4082305009,"location":{"name":"Atlanta, Georgia"},"metadata":null,"id":4121279009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"147","title":"Nurse Practitioner or Physician Assistant","company_name":"Headlands Research","first_published":"2026-02-11T17:12:30-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us - it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our clinical research site located in Stockbridge, GA. \u0026lt;strong\u0026gt;The site is expanding our therapeutic areas to include CNS related conditions. We are ideally seeking an advanced provider with experience working in this space.\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Atlanta, a Headlands Research site, is a leading multi-specialty research center with a long-standing reputation for excellence. The site has delivered more than 300 clinical trials across a wide range of therapeutic areas, including addiction, dermatology, infectious diseases, and more.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Part Time Employee, Flexible Schedule\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as an Investigator in clinical research.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Stockbridge, GA (no opportunities for remote or hybrid)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; (Part Time) within Mondays through Thursdays, 7:30am - 5:30pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety and welfare of each study subject\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have in-depth knowledge of all research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct medical history interviews and physical examinations throughout the subject’s study participation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review EKG’s and lab results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical care as needed during a subject’s participation in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide home based on-call availability per Artemis standard policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend Investigator Meetings on behalf of Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent professional communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Friendly and outgoing demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must demonstrate a passion for direct patient interaction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CNS experience strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an NP or PA in the state of Georgia required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within the clinical research industry highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4183294009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4106163009,"location":{"name":"Scottsdale, Arizona"},"metadata":null,"id":4183294009,"updated_at":"2026-06-05T17:14:18-04:00","requisition_id":"186","title":"Nurse Practitioner or Physician Assistant","company_name":"Headlands Research","first_published":"2026-03-13T17:07:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;job__header\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;job__title\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;job__description body\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us - it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our clinical research site located in Scottsdale, AZ. You will help the site conduct clinical research trials involving CNS, psych, musculoskeletal, addiction, vaccines, and general medicine. They are known for their integration of technology to streamline processes for their Sponsor/CRO partners and most importantly subjects.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Headlands Research Scottsdale is a premier clinical research site in the Phoenix region. Strategically located in a diverse metro area that is home to vibrant communities, the site excels in rapid participant recruitment and high-quality, patient-centered research. Headlands Research Scottsdale partners with pharmaceutical sponsors and CROs to advance innovative therapies while upholding the highest standards of care and compliance.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time Regular Employee\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as an Investigator in clinical research and years of experience as an advanced provider.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Scottsdale, AZ (no opportunities for remote or hybrid)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026amp;nbsp;Mondays through Fridays, 8:00am-5:00pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety and welfare of each study subject\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have in-depth knowledge of all research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct medical history interviews and physical examinations throughout the subject’s study participation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review EKG’s and lab results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical care as needed during a subject’s participation in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide home based on-call availability per site policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend Investigator Meetings on behalf of Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent professional communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Friendly and outgoing demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must demonstrate a passion for direct patient interaction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an NP or PA in the state of Arizona required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within the clinical research industry highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004740009,"name":"Arizona - Scottsdale","location":"Scottsdale, Arizona, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4208830009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4122228009,"location":{"name":"Myrtle Beach, South Carolina"},"metadata":null,"id":4208830009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"214","title":"Nurse Practitioner or Physician Assistant - Clinical Research","company_name":"Headlands Research","first_published":"2026-04-09T10:55:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking a full-time experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our Trial Management Associate site located in Myrtle Beach, SC.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time Regular Employee\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as an APP and as an investigator in clinical research.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Myrtle Beach, SC (no opportunities for remote or hybrid)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Mondays through Thursdays 7:00am - 4:30pm, Fridays 7:30am - 11:30am\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety and welfare of each study subject\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have in-depth knowledge of all research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct medical history interviews and physical examinations throughout the subject’s study participation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review EKG’s and lab results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical care as needed during a subject’s participation in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide home based on-call availability per site policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend Investigator Meetings on behalf of Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent professional communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Friendly and outgoing demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must demonstrate a passion for direct patient interaction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an NP or PA in the state of South Carolina required (or eligible for)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within the clinical research industry preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004753009,"name":"South Carolina - Myrtle Beach","location":"Myrtle Beach, South Carolina, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4246708009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4144099009,"location":{"name":"Plymouth, Massachusetts"},"metadata":null,"id":4246708009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"252","title":"Nurse Practitioner or Physician Assistant - Plymouth, MA - Clinical Research","company_name":"Headlands Research","first_published":"2026-05-21T17:40:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1tw2tfc\u0026quot; data-start=\u0026quot;0\u0026quot; data-end=\u0026quot;43\u0026quot;\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;45\u0026quot; data-end=\u0026quot;458\u0026quot;\u0026gt;At \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;48\u0026quot; data-end=\u0026quot;122\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt;, diversity is not just a goal — it is foundational to how we advance medicine. We are committed to improving representation in clinical research and ensuring patients from all backgrounds have access to innovative treatment opportunities. From the patients we serve to the teams we build, inclusivity is embedded into everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;618\u0026quot; data-end=\u0026quot;652\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;19cyuv5\u0026quot; data-start=\u0026quot;654\u0026quot; data-end=\u0026quot;714\u0026quot;\u0026gt;Make a Meaningful Impact in Dementia \u0026amp;amp; Neurology Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;1080\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearchema.com/?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;816\u0026quot;\u0026gt;Headlands Research Eastern Massachusetts\u0026lt;/a\u0026gt;, in partnership with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;838\u0026quot; data-end=\u0026quot;918\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt;, is seeking an experienced Nurse Practitioner or Physician Assistant to join our growing clinical research team as a Sub-Investigator in Plymouth, Massachusetts.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1082\u0026quot; data-end=\u0026quot;1383\u0026quot;\u0026gt;This role is ideal for an advanced provider who is passionate about caring for adult and geriatric patients - particularly those affected by Alzheimer’s disease, dementia, and other neurological conditions - and who wants to play a direct role in advancing future treatments through clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1385\u0026quot; data-end=\u0026quot;1615\u0026quot;\u0026gt;We are especially interested in connecting with providers who live within a commutable distance to Plymouth and who value building strong relationships with patients and caregivers in a collaborative, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;Why Join Us?\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r7878a\u0026quot; data-start=\u0026quot;1639\u0026quot; data-end=\u0026quot;1679\u0026quot;\u0026gt;Meaningful Work in Dementia Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1680\u0026quot; data-end=\u0026quot;1847\u0026quot;\u0026gt;Help bring innovative therapies to patients living with Alzheimer’s disease and related dementias while supporting families navigating complex neurological conditions.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;80ghtc\u0026quot; data-start=\u0026quot;1849\u0026quot; data-end=\u0026quot;1896\u0026quot;\u0026gt;Collaborative Neurology-Focused Environment\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1897\u0026quot; data-end=\u0026quot;2078\u0026quot;\u0026gt;Work alongside experienced neurologists, clinical research coordinators, raters, and patient recruitment specialists as part of both Headlands Research and Seacoast Neurology Group.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;107ic8x\u0026quot; data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2254\u0026quot;\u0026gt;Supportive, High-Performing Culture\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;2255\u0026quot; data-end=\u0026quot;2480\u0026quot;\u0026gt;Our teams value professionalism, accountability, compassion, and collaboration. You will be supported by experienced research staff while having the opportunity to grow your clinical research experience and leadership skills.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Location: \u0026amp;nbsp; \u0026lt;/strong\u0026gt;Onsite in Plymouth, Massachusetts (no remote or hybrid opportunities)\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Schedule:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Full-Time | Monday through Friday\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Pay:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$120,000 - 140,000/yr (dependent upon years of experience, certifications, and education)\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;Responsibilities:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;6hqsmy\u0026quot; data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;2940\u0026quot;\u0026gt;Ensure the safety and welfare of clinical trial participants\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;tkipd6\u0026quot; data-start=\u0026quot;2941\u0026quot; data-end=\u0026quot;3000\u0026quot;\u0026gt;Conduct medical history reviews and physical examinations\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1arrgwj\u0026quot; data-start=\u0026quot;3001\u0026quot; data-end=\u0026quot;3091\u0026quot;\u0026gt;Evaluate potential study participants according to protocol inclusion/exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;c50yt0\u0026quot; data-start=\u0026quot;3092\u0026quot; data-end=\u0026quot;3157\u0026quot;\u0026gt;Review EKGs, laboratory results, and other clinical assessments\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;14sy18i\u0026quot; data-start=\u0026quot;3158\u0026quot; data-end=\u0026quot;3225\u0026quot;\u0026gt;Provide medical oversight and care throughout study participation\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xox3k8\u0026quot; data-start=\u0026quot;3226\u0026quot; data-end=\u0026quot;3324\u0026quot;\u0026gt;Develop strong rapport with dementia patients and caregivers through compassionate communication\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1914vgm\u0026quot; data-start=\u0026quot;3325\u0026quot; data-end=\u0026quot;3416\u0026quot;\u0026gt;Collaborate closely with neurologists, research coordinators, and sponsor representatives\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8mm6up\u0026quot; data-start=\u0026quot;3417\u0026quot; data-end=\u0026quot;3477\u0026quot;\u0026gt;Maintain in-depth knowledge of assigned research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;9f28cy\u0026quot; data-start=\u0026quot;3478\u0026quot; data-end=\u0026quot;3558\u0026quot;\u0026gt;Attend Investigator Meetings on behalf of the Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1wfhkz3\u0026quot; data-start=\u0026quot;3559\u0026quot; data-end=\u0026quot;3621\u0026quot;\u0026gt;Support high-quality data collection and protocol compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;18ypsib\u0026quot; data-start=\u0026quot;3622\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;Demonstrate professionalism, accountability, and strong patient-centered communication\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;Requirements:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;nuseyd\u0026quot; data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;3835\u0026quot;\u0026gt;Minimum of 2 years of experience as a licensed Nurse Practitioner or Physician Assistant preferred; willing to consider new graduates\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1io90kj\u0026quot; data-start=\u0026quot;3836\u0026quot; data-end=\u0026quot;3918\u0026quot;\u0026gt;Current and unencumbered NP or PA license in the state of Massachusetts required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;vmz64g\u0026quot; data-start=\u0026quot;3919\u0026quot; data-end=\u0026quot;3993\u0026quot;\u0026gt;Experience working with adult and geriatric patient populations required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;j5uwn4\u0026quot; data-start=\u0026quot;3994\u0026quot; data-end=\u0026quot;4159\u0026quot;\u0026gt;Prior experience caring for patients with dementia, Alzheimer’s disease, neurology, geriatrics, psychiatry, primary care, or related specialties strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;ehkut2\u0026quot; data-start=\u0026quot;4160\u0026quot; data-end=\u0026quot;4218\u0026quot;\u0026gt;Clinical research experience preferred, but not required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;156lb62\u0026quot; data-start=\u0026quot;4219\u0026quot; data-end=\u0026quot;4342\u0026quot;\u0026gt;Strong interpersonal skills with the ability to communicate effectively with cognitively impaired patients and caregivers\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;5sxdnd\u0026quot; data-start=\u0026quot;4343\u0026quot; data-end=\u0026quot;4393\u0026quot;\u0026gt;Highly organized with strong attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;yt3tga\u0026quot; data-start=\u0026quot;4394\u0026quot; data-end=\u0026quot;4448\u0026quot;\u0026gt;Professional, dependable, and collaborative demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;41qls8\u0026quot; data-start=\u0026quot;4449\u0026quot; data-end=\u0026quot;4520\u0026quot;\u0026gt;Passion for direct patient interaction and advancing medical research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;lm26i9\u0026quot; data-start=\u0026quot;4521\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;Ability to thrive in a fast-paced, team-oriented clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;About Headlands Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;5037\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;4702\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt; is a leading integrated clinical trial site network with a mission to improve lives by advancing innovative medical therapies. Our sites partner with sponsors and CROs to conduct high-quality clinical trials across a variety of therapeutic areas while delivering exceptional patient care and operational excellence.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5039\u0026quot; data-end=\u0026quot;5273\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;At our Eastern Massachusetts site, we are proud to partner closely with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;5111\u0026quot; data-end=\u0026quot;5191\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt; to advance neurological and dementia-focused research within the local community.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4257212009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4144099009,"location":{"name":"Plymouth, Massachusetts"},"metadata":null,"id":4257212009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"252","title":"Nurse Practitioner - Plymouth, MA - Clinical Research","company_name":"Headlands Research","first_published":"2026-05-21T17:41:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1tw2tfc\u0026quot; data-start=\u0026quot;0\u0026quot; data-end=\u0026quot;43\u0026quot;\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;45\u0026quot; data-end=\u0026quot;458\u0026quot;\u0026gt;At \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;48\u0026quot; data-end=\u0026quot;122\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt;, diversity is not just a goal — it is foundational to how we advance medicine. We are committed to improving representation in clinical research and ensuring patients from all backgrounds have access to innovative treatment opportunities. From the patients we serve to the teams we build, inclusivity is embedded into everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;618\u0026quot; data-end=\u0026quot;652\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;19cyuv5\u0026quot; data-start=\u0026quot;654\u0026quot; data-end=\u0026quot;714\u0026quot;\u0026gt;Make a Meaningful Impact in Dementia \u0026amp;amp; Neurology Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;1080\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearchema.com/?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;816\u0026quot;\u0026gt;Headlands Research Eastern Massachusetts\u0026lt;/a\u0026gt;, in partnership with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;838\u0026quot; data-end=\u0026quot;918\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt;, is seeking an experienced Nurse Practitioner or Physician Assistant to join our growing clinical research team as a Sub-Investigator in Plymouth, Massachusetts.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1082\u0026quot; data-end=\u0026quot;1383\u0026quot;\u0026gt;This role is ideal for an advanced provider who is passionate about caring for adult and geriatric patients - particularly those affected by Alzheimer’s disease, dementia, and other neurological conditions - and who wants to play a direct role in advancing future treatments through clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1385\u0026quot; data-end=\u0026quot;1615\u0026quot;\u0026gt;We are especially interested in connecting with providers who live within a commutable distance to Plymouth and who value building strong relationships with patients and caregivers in a collaborative, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;Why Join Us?\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r7878a\u0026quot; data-start=\u0026quot;1639\u0026quot; data-end=\u0026quot;1679\u0026quot;\u0026gt;Meaningful Work in Dementia Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1680\u0026quot; data-end=\u0026quot;1847\u0026quot;\u0026gt;Help bring innovative therapies to patients living with Alzheimer’s disease and related dementias while supporting families navigating complex neurological conditions.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;80ghtc\u0026quot; data-start=\u0026quot;1849\u0026quot; data-end=\u0026quot;1896\u0026quot;\u0026gt;Collaborative Neurology-Focused Environment\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1897\u0026quot; data-end=\u0026quot;2078\u0026quot;\u0026gt;Work alongside experienced neurologists, clinical research coordinators, raters, and patient recruitment specialists as part of both Headlands Research and Seacoast Neurology Group.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;107ic8x\u0026quot; data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2254\u0026quot;\u0026gt;Supportive, High-Performing Culture\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;2255\u0026quot; data-end=\u0026quot;2480\u0026quot;\u0026gt;Our teams value professionalism, accountability, compassion, and collaboration. You will be supported by experienced research staff while having the opportunity to grow your clinical research experience and leadership skills.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Location: \u0026amp;nbsp; \u0026lt;/strong\u0026gt;Onsite in Plymouth, Massachusetts (no remote or hybrid opportunities)\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Schedule:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Full-Time | Monday through Friday\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Pay:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$120,000 - 140,000/yr (dependent upon years of experience, certifications, and education)\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;Responsibilities:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;6hqsmy\u0026quot; data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;2940\u0026quot;\u0026gt;Ensure the safety and welfare of clinical trial participants\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;tkipd6\u0026quot; data-start=\u0026quot;2941\u0026quot; data-end=\u0026quot;3000\u0026quot;\u0026gt;Conduct medical history reviews and physical examinations\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1arrgwj\u0026quot; data-start=\u0026quot;3001\u0026quot; data-end=\u0026quot;3091\u0026quot;\u0026gt;Evaluate potential study participants according to protocol inclusion/exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;c50yt0\u0026quot; data-start=\u0026quot;3092\u0026quot; data-end=\u0026quot;3157\u0026quot;\u0026gt;Review EKGs, laboratory results, and other clinical assessments\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;14sy18i\u0026quot; data-start=\u0026quot;3158\u0026quot; data-end=\u0026quot;3225\u0026quot;\u0026gt;Provide medical oversight and care throughout study participation\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xox3k8\u0026quot; data-start=\u0026quot;3226\u0026quot; data-end=\u0026quot;3324\u0026quot;\u0026gt;Develop strong rapport with dementia patients and caregivers through compassionate communication\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1914vgm\u0026quot; data-start=\u0026quot;3325\u0026quot; data-end=\u0026quot;3416\u0026quot;\u0026gt;Collaborate closely with neurologists, research coordinators, and sponsor representatives\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8mm6up\u0026quot; data-start=\u0026quot;3417\u0026quot; data-end=\u0026quot;3477\u0026quot;\u0026gt;Maintain in-depth knowledge of assigned research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;9f28cy\u0026quot; data-start=\u0026quot;3478\u0026quot; data-end=\u0026quot;3558\u0026quot;\u0026gt;Attend Investigator Meetings on behalf of the Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1wfhkz3\u0026quot; data-start=\u0026quot;3559\u0026quot; data-end=\u0026quot;3621\u0026quot;\u0026gt;Support high-quality data collection and protocol compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;18ypsib\u0026quot; data-start=\u0026quot;3622\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;Demonstrate professionalism, accountability, and strong patient-centered communication\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;Requirements:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;nuseyd\u0026quot; data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;3835\u0026quot;\u0026gt;Minimum of 2 years of experience as a licensed Nurse Practitioner or Physician Assistant preferred; willing to consider new graduates\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1io90kj\u0026quot; data-start=\u0026quot;3836\u0026quot; data-end=\u0026quot;3918\u0026quot;\u0026gt;Current and unencumbered NP or PA license in the state of Massachusetts required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;vmz64g\u0026quot; data-start=\u0026quot;3919\u0026quot; data-end=\u0026quot;3993\u0026quot;\u0026gt;Experience working with adult and geriatric patient populations required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;j5uwn4\u0026quot; data-start=\u0026quot;3994\u0026quot; data-end=\u0026quot;4159\u0026quot;\u0026gt;Prior experience caring for patients with dementia, Alzheimer’s disease, neurology, geriatrics, psychiatry, primary care, or related specialties strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;ehkut2\u0026quot; data-start=\u0026quot;4160\u0026quot; data-end=\u0026quot;4218\u0026quot;\u0026gt;Clinical research experience preferred, but not required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;156lb62\u0026quot; data-start=\u0026quot;4219\u0026quot; data-end=\u0026quot;4342\u0026quot;\u0026gt;Strong interpersonal skills with the ability to communicate effectively with cognitively impaired patients and caregivers\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;5sxdnd\u0026quot; data-start=\u0026quot;4343\u0026quot; data-end=\u0026quot;4393\u0026quot;\u0026gt;Highly organized with strong attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;yt3tga\u0026quot; data-start=\u0026quot;4394\u0026quot; data-end=\u0026quot;4448\u0026quot;\u0026gt;Professional, dependable, and collaborative demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;41qls8\u0026quot; data-start=\u0026quot;4449\u0026quot; data-end=\u0026quot;4520\u0026quot;\u0026gt;Passion for direct patient interaction and advancing medical research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;lm26i9\u0026quot; data-start=\u0026quot;4521\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;Ability to thrive in a fast-paced, team-oriented clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;About Headlands Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;5037\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;4702\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt; is a leading integrated clinical trial site network with a mission to improve lives by advancing innovative medical therapies. Our sites partner with sponsors and CROs to conduct high-quality clinical trials across a variety of therapeutic areas while delivering exceptional patient care and operational excellence.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5039\u0026quot; data-end=\u0026quot;5273\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;At our Eastern Massachusetts site, we are proud to partner closely with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;5111\u0026quot; data-end=\u0026quot;5191\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt; to advance neurological and dementia-focused research within the local community.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4245281009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4143192009,"location":{"name":"Baltimore, Maryland"},"metadata":null,"id":4245281009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"250","title":"Part-time or Full-time Physician - Clinical Research","company_name":"Headlands Research","first_published":"2026-05-21T16:50:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Pharmasite Research, located in the greater Baltimore area, is a dedicated clinical research site with over twenty years of experience across multiple therapeutic areas, with a particular focus on mental health and central nervous system (CNS) conditions. The site is committed to delivering high-quality, patient-centered research, prioritizing participant care, safety, and study integrity. With an experienced team serving a diverse population, Pharmasite Research partners with sponsors and CROs to advance innovative therapies and improve health outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference?\u0026amp;nbsp;With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an MD or DO within the state of Maryland required (or eligible for).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4061298009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4041368009,"location":{"name":"Riverside, California"},"metadata":null,"id":4061298009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"81","title":"Part-time Psychiatrist - Clinical Research","company_name":"Headlands Research","first_published":"2025-11-19T09:48:05-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking a \u0026lt;strong\u0026gt;part-time\u0026lt;/strong\u0026gt; experienced \u0026lt;strong\u0026gt;psychiatrist \u0026lt;/strong\u0026gt;to help us grow our clinical research site at Artemis Institute for Clinical Research in \u0026lt;strong\u0026gt;Riverside\u0026lt;/strong\u0026gt;, CA. Ideally, this person would work up to any 3 days per week Monday through Thursday, during the hours of 8:00am to 2:00pm.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials is a huge plus, but willing to consider those without.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eligible for or active unencumbered license to practice as an MD or DO within the state of California required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4239385009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4139868009,"location":{"name":"Rolling Hills Estates, California"},"metadata":null,"id":4239385009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"245","title":"Patient-facing Research Assistant","company_name":"Headlands Research","first_published":"2026-05-06T17:29:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p data-start=\u0026quot;167\u0026quot; data-end=\u0026quot;247\u0026quot;\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Rolling Hills Estates, CA\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;500\u0026quot; data-end=\u0026quot;503\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;506\u0026quot; data-end=\u0026quot;558\u0026quot;\u0026gt;Peninsula Research Associates\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;558\u0026quot; data-end=\u0026quot;561\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Full-Time | Monday through Friday | 8:00am - 5:00pm\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;Launch Your Career in Healthcare \u0026amp;amp; Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;299\u0026quot; data-end=\u0026quot;612\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;268\u0026quot; data-end=\u0026quot;528\u0026quot;\u0026gt;Are you a recent graduate looking to gain hands-on experience in healthcare or clinical research? This is an exciting opportunity to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;530\u0026quot; data-end=\u0026quot;935\u0026quot;\u0026gt;As a \u0026lt;strong data-start=\u0026quot;535\u0026quot; data-end=\u0026quot;566\u0026quot;\u0026gt;Clinical Research Assistant\u0026lt;/strong\u0026gt;, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you\u0026#39;re planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;299\u0026quot; data-end=\u0026quot;612\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;951\u0026quot; data-end=\u0026quot;954\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;xti9y5\u0026quot; data-start=\u0026quot;956\u0026quot; data-end=\u0026quot;976\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;xti9y5\u0026quot; data-start=\u0026quot;956\u0026quot; data-end=\u0026quot;976\u0026quot;\u0026gt;What You’ll Do\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Study Preparation\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participant Care and Interaction\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with participant stipend tracking and processing.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Laboratory and Specimen Handling\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and file weekly temperature reports for laboratory systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Entry and Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administrative and General Support\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings, study teleconferences, and trainings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with onsite or remote clinical research monitor visits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1487\u0026quot; data-end=\u0026quot;1490\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1f5kc01\u0026quot; data-start=\u0026quot;1492\u0026quot; data-end=\u0026quot;1524\u0026quot;\u0026gt;What Makes You a Great Fit\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and ability to follow step-by-step procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work efficiently in a fast-paced environment with changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills and a professional, patient-focused demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable interacting with a diverse patient population\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, dependable, and eager to learn new skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance multiple tasks and priorities throughout the day\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional, reliable, and eager to learn\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2035\u0026quot; data-end=\u0026quot;2038\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Requirements\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2393\u0026quot;\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;CNAs, Medical Assistants, Phlebotomists, and other patient-care healthcare roles heavily preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with medical terminology and laboratory procedures preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, with the ability to collect, compile, and analyze patient data accurately.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, communication (verbal and written), and customer service skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Easily able to learn new computer or website applications (i.e. Electronic Medical Records, Clinial Trial Management Systems, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to prioritize tasks, meet deadlines, and adapt to a fast-paced work environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving skills with a proactive and solution-oriented approach.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills with the proven ability to prioritize tasks and meet strict deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xrynm\u0026quot; data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2100\u0026quot;\u0026gt;Phlebotomy training and experience heavily preferred; willingness to become fully trained required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2395\u0026quot; data-end=\u0026quot;2398\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;iyhmpw\u0026quot; data-start=\u0026quot;2400\u0026quot; data-end=\u0026quot;2441\u0026quot;\u0026gt;Why This Role is a Great First Step\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;wylw1b\u0026quot; data-start=\u0026quot;3300\u0026quot; data-end=\u0026quot;3381\u0026quot;\u0026gt;Gain hands-on experience working directly with patients in a clinical setting\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;16gzdnb\u0026quot; data-start=\u0026quot;3382\u0026quot; data-end=\u0026quot;3458\u0026quot;\u0026gt;Learn the fundamentals of clinical research and how trials are conducted\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1o8ku67\u0026quot; data-start=\u0026quot;3459\u0026quot; data-end=\u0026quot;3542\u0026quot;\u0026gt;Build transferable skills for careers in healthcare, research, or biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;4waw5a\u0026quot; data-start=\u0026quot;3543\u0026quot; data-end=\u0026quot;3623\u0026quot;\u0026gt;Work alongside experienced professionals who provide training and mentorship\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1on929o\u0026quot; data-start=\u0026quot;3624\u0026quot; data-end=\u0026quot;3726\u0026quot;\u0026gt;Create a strong foundation for advancement into roles like Clinical Research Coordinator or beyond\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;uvrqhh\u0026quot; data-start=\u0026quot;3727\u0026quot; data-end=\u0026quot;3813\u0026quot;\u0026gt;Make a meaningful impact by helping bring new treatments and therapies to patients\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2768\u0026quot; data-end=\u0026quot;2771\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2773\u0026quot; data-end=\u0026quot;2928\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;If you\u0026#39;re looking to turn your academic experience into a meaningful, patient-focused career, this is a powerful place to start.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$22\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$27 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4212302009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4124549009,"location":{"name":"Richmond, British Columbia"},"metadata":null,"id":4212302009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"217","title":"Patient Recruitment Specialist","company_name":"Headlands Research","first_published":"2026-04-09T22:09:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Patient Recruitment Specialist responsible for all recruitment related activities for assigned clinical trials. This includes but is not limited to outstanding customer service skills, an in-depth knowledge of protocol specific inclusion/exclusion criteria, participation in the development of recruitment strategies and plans, and the tracking of recruitment results. The Patient Recruitment Specialist will mainly be responsible for phone screening potential study participants, entering information into the clinical database, and scheduling potential participants for on-site visits. In addition, the Patient Recruitment Specialist is required to have an in-depth knowledge of good clinical practices and privacy regulations as set forth by federal and provincial regulations.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain a thorough understanding of assigned study inclusion/exclusion criteria.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Make outgoing calls and answer incoming calls from potential study patients and assess preliminary subject eligibility against protocol specific inclusion and exclusion criteria and utilize these criteria to effectively assess potential participants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Follow recruitment follow up processes thoroughly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review patient database to identify potential study patients and initiate contact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure accurate collection and entry of patient information into our database.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure courteous and efficient service is provided to all potential participants.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use effective communication and report daily to the study team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain relationships with Family Doctor’s and specialists in the community.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use the electronic database to book study visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and report at weekly team meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan, organize, and attend community outreach events.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Send recruitment update emails to email database.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Send faxes to Family Doctor’s regarding ongoing studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contact patients from physician referrals within 24 hours of referral receipt\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Comfortable using medical terminology.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent customer service.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verbal and written communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Planning/organization skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong ability to work independently.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to multi-task.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in MS Word, MS Excel, and MS Outlook.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Computer literacy required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Job Status:\u0026lt;/strong\u0026gt; Full Time / 40 hours per week\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Salary\u0026lt;/strong\u0026gt;: $52,000 - $56,000\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Employee benefits:\u0026lt;/strong\u0026gt; Eligible after 3-month probation period.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule\u0026lt;/strong\u0026gt;: Monday to Friday 8:00am – 4:30pm (Onsite)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005114009,"name":"Marketing \u0026 Patient Recruitment","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004755009,"name":"Canada - Richmond, BC","location":"Richmond, British Columbia, Canada","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4215386009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4126331009,"location":{"name":"Remote"},"metadata":null,"id":4215386009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"220","title":"Patient Recruitment Specialist","company_name":"Headlands Research","first_published":"2026-04-13T10:25:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Under the supervision of the Patient Recruitment Manager, the Patient Recruitment Specialist will work remotely and be responsible for all recruitment related activities for assigned clinical trials. This includes but is not limited to mastery of protocol specific inclusion/exclusion criteria, participation in the development of recruitment strategies and plans, and the tracking of recruitment results. The Patient Recruitment Specialist will mainly be responsible for phone screening potential study participants, entering information into the clinical database, and scheduling potential participants for on-site visits.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Duties/Responsibilities \u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Make 60+ outbound calls a day, responding to patients that are interested in participating in a clinical trial; assess preliminary subject eligibility against protocol specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Answer incoming calls from potential study patients and assess preliminary subject eligibility against protocol specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pass qualified patients onto the Sr. Patient Recruitment Specialist for more detailed medical pre-screening\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain working knowledge of assigned medical indications\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review patient database, vendor portals and other electronic platforms as required to identify potential study patients and initiate contact\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure accurate collection and entry of patient information into the relevant databases while on the phone\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure courteous and efficient service is provided to all callers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other members of your team as well as cross-functional team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend and contribute to department meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Performing other administrative tasks, as required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree, Associate’s degree or equivalent preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience delivering excellent customer service is required; call center experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical terminology knowledge a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bilingual (Spanish/English) a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior inside sales experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Salesforce a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Passion for communicating to people\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possess exceptional organizational skills and attention to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Display excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to quickly adapt to changes in responsibilities, workloads and priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be a fast learner with capacity to retain and differentiate key enrollment criteria across clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate a focus on process improvement and be capable of articulating ideas for improving efficiency and maximizing results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possess well-developed interpersonal skills and an ability to work well independently, as well as with co-workers, peers, supervisor and external customers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to maintain confidentiality with HIPAA guidelines, patient information and other sensitive information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate professionalism, sense of urgency and self-motivation to achieve required metrics\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005114009,"name":"Marketing \u0026 Patient Recruitment","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4258718009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4151335009,"location":{"name":"San Diego, California"},"metadata":null,"id":4258718009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"261","title":"Pharmacy Technician","company_name":"Headlands Research","first_published":"2026-05-27T14:37:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;📍 San Diego, CA\u0026lt;br data-start=\u0026quot;687\u0026quot; data-end=\u0026quot;690\u0026quot;\u0026gt;🏥 Artemis Institute for Clinical Research\u0026lt;br data-start=\u0026quot;748\u0026quot; data-end=\u0026quot;751\u0026quot;\u0026gt;🕒 Full-time | Onsite (no opportunities for hybrid or remote)\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;794\u0026quot; data-end=\u0026quot;876\u0026quot;\u0026gt;For experienced Pharmacy Technicians looking for meaningful work in clinical research.\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;259\u0026quot; data-end=\u0026quot;462\u0026quot;\u0026gt;If you’re a Pharmacy Technician who values precision, compliance, patient safety, and collaborative clinical environments, Artemis San Diego\u0026amp;nbsp;may be the right next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;464\u0026quot; data-end=\u0026quot;823\u0026quot;\u0026gt;Our San Diego site is known for its strong operational infrastructure, experienced research teams, and commitment to advancing metabolic and immunologic research through high-quality clinical trials. This role offers the opportunity to work directly with investigational products and contribute to studies that support the development of innovative therapies.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced Pharmacy Technicians Choose US\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1d0z8va\u0026quot; data-start=\u0026quot;1623\u0026quot; data-end=\u0026quot;1704\u0026quot;\u0026gt;Exposure to complex investigational product management within clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;hxkrw5\u0026quot; data-start=\u0026quot;1705\u0026quot; data-end=\u0026quot;1797\u0026quot;\u0026gt;Collaborative environment with experienced investigators, coordinators, and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;jgkz2w\u0026quot; data-start=\u0026quot;1798\u0026quot; data-end=\u0026quot;1866\u0026quot;\u0026gt;Strong operational support, SOPs, and compliance-focused processes\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;hc0qv9\u0026quot; data-start=\u0026quot;1867\u0026quot; data-end=\u0026quot;1942\u0026quot;\u0026gt;Opportunity to contribute to meaningful metabolic and immunologic studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1ymmsxp\u0026quot; data-start=\u0026quot;1943\u0026quot; data-end=\u0026quot;2021\u0026quot;\u0026gt;Backing of a growing research network with resources and long-term stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for Pharmacy Technicians who enjoy working in highly regulated environments, take pride in accuracy and documentation, and want to be part of a team advancing innovative medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Pharmacy Technician plays a key role in the successful execution of clinical trials by ensuring the safe, accurate, and compliant handling of investigational products (IP). Working under the supervision of a licensed pharmacist or certified technician (as applicable), this individual will be responsible for receiving, storing, preparing, dispensing, documenting, and managing investigational drugs in accordance with study protocols, GCP/ICH regulations, and institutional SOPs. This role may also support administrative and data entry activities related to the conduct of clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Investigational Product (IP) Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Receive, store, prepare, and dispense investigational products according to protocol, pharmacy manual, and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use IWRS/IRT systems to log shipments, assign IP, and perform returns or destructions per study-specific guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate inventory logs, temperature records, and expiration tracking for all IP and supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and respond to temperature excursions, discrepancies, or deviations per SOP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform aseptic preparations where required, following sterile technique protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage IP accountability documentation, including blinded and unblinded logs and reconciliation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all investigational product storage complies with GCP and institutional policies (double-locked, secure, labeled, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Documentation \u0026amp;amp; Compliance\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain audit-ready records of all pharmacy activities, including temperature logs, equipment calibrations, and IP logs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create and manage pharmacy study binders with updated regulatory and protocol-specific content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to ALCOA-C principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, and Consistent) in documentation practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administrative \u0026amp;amp; Operational Support\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist with scheduling and performing protocol-specific assessments (e.g., memory assessments, vital signs, specimen collection support).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform data entry in eCRFs according to protocol and system-specific guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support query resolution, documentation scanning, and other clerical duties (e.g., faxing, reminder calls).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Order pharmacy-related supplies and assist with equipment upkeep and calibrations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide pharmacy support to other team members and backfill duties during absences.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communication \u0026amp;amp; Collaboration\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain clear, professional communication with study coordinators, monitors, sponsors, and clinical staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in team meetings and training sessions to stay updated on protocols, SOPs, and compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate flexibility and professionalism in a fast-paced, regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Completion of a recognized Pharmacy Technician program preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Registration with relevant state or provincial licensing body (e.g., College of Pharmacists of BC) required where applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current certification in Good Clinical Practice (GCP) and/or willingness to complete GCP training.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 1–2 years of experience as a Pharmacy Technician, preferably in a clinical research or hospital setting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with IWRS/IRT systems, inventory control, and investigational product handling preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Phase I–IV clinical trials and regulatory requirements an asset.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational and documentation skills with high attention to detail.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and electronic data capture systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to follow protocols, SOPs, and maintain regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple tasks efficiently and work independently or as part of a team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professionalism, reliability, and commitment to patient safety and data integrity.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1330\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1333\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;About Artemis Institute for Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;Artemis Institute for Clinical Research – San Diego brings together an award-winning team and a strong commitment to its core purpose and values to deliver a thoughtful, patient-centered approach to clinical research. Having conducted more than 315 successful trials across over 20 therapeutic areas, the site has earned a reputation for excellence and reliability. Artemis San Diego partners with sponsors and CROs to advance innovative therapies while upholding the highest standards of quality, professionalism, and care.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;qMYqUG_convSearchResultHighlightRoot\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;\u0026quot; data-turn-id-container=\u0026quot;request-WEB:bf2b4374-f977-4718-8018-f84b55cba826-0\u0026quot; data-is-intersecting=\u0026quot;true\u0026quot;\u0026gt;\n\u0026lt;section class=\u0026quot;text-token-text-primary w-full focus:outline-none has-data-writing-block:pointer-events-none [\u0026amp;amp;:has([data-writing-block])\u0026gt;*]:pointer-events-auto R6Vx5W_threadScrollVars scroll-mb-[calc(var(--scroll-root-safe-area-inset-bottom,0px)+var(--thread-response-height))] scroll-mt-[calc(var(--header-height)+min(200px,max(70px,20svh)))]\u0026quot; data-turn-id=\u0026quot;request-WEB:bf2b4374-f977-4718-8018-f84b55cba826-0\u0026quot; data-turn-id-container=\u0026quot;request-WEB:bf2b4374-f977-4718-8018-f84b55cba826-0\u0026quot; data-testid=\u0026quot;conversation-turn-2\u0026quot; data-scroll-anchor=\u0026quot;false\u0026quot; data-turn=\u0026quot;assistant\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;text-base my-auto mx-auto pb-10 [--thread-content-margin:var(--thread-content-margin-xs,calc(var(--spacing)*4))] @w-sm/main:[--thread-content-margin:var(--thread-content-margin-sm,calc(var(--spacing)*6))] @w-lg/main:[--thread-content-margin:var(--thread-content-margin-lg,calc(var(--spacing)*16))] px-(--thread-content-margin)\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;[--thread-content-max-width:40rem] @w-lg/main:[--thread-content-max-width:48rem] mx-auto max-w-(--thread-content-max-width) flex-1 group/turn-messages focus-visible:outline-hidden relative flex w-full min-w-0 flex-col agent-turn\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;flex max-w-full flex-col gap-4 grow\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;min-h-8 text-message relative flex w-full flex-col items-end gap-2 text-start break-words whitespace-normal outline-none keyboard-focused:focus-ring [.text-message+\u0026amp;amp;]:mt-1\u0026quot; data-message-author-role=\u0026quot;assistant\u0026quot; data-message-id=\u0026quot;e94c3f9f-e38f-4bfe-9db4-6cba19bbb8d9\u0026quot; data-message-model-slug=\u0026quot;gpt-5-5\u0026quot; data-turn-start-message=\u0026quot;true\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;flex w-full flex-col gap-1 empty:hidden\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;markdown prose dark:prose-invert wrap-break-word w-full light markdown-new-styling\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1hqcdaf\u0026quot; data-start=\u0026quot;5412\u0026quot; data-end=\u0026quot;5439\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;5441\u0026quot; data-end=\u0026quot;5856\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;swtf0u\u0026quot; data-start=\u0026quot;5441\u0026quot; data-end=\u0026quot;5514\u0026quot;\u0026gt;Pharmacy Technicians who value structure, precision, and accountability\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;iledk0\u0026quot; data-start=\u0026quot;5515\u0026quot; data-end=\u0026quot;5599\u0026quot;\u0026gt;Professionals interested in transitioning into or growing within clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1atnhah\u0026quot; data-start=\u0026quot;5600\u0026quot; data-end=\u0026quot;5685\u0026quot;\u0026gt;Individuals who enjoy detailed documentation and investigational product management\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;145nixn\u0026quot; data-start=\u0026quot;5686\u0026quot; data-end=\u0026quot;5766\u0026quot;\u0026gt;Team-oriented professionals who value collaboration and operational excellence\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;yorokd\u0026quot; data-start=\u0026quot;5767\u0026quot; data-end=\u0026quot;5856\u0026quot;\u0026gt;Those motivated by contributing to innovative therapies and meaningful patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;5860\u0026quot; data-end=\u0026quot;6064\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;📬 Apply today if you’re looking for a Pharmacy Technician role where your attention to detail, compliance expertise, and operational support directly contribute to advancing meaningful clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;opacity-100 transition-opacity duration-300 ease-out motion-reduce:transition-none starting:opacity-0\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;border-token-border-default mt-2 border-t py-4 text-sm\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/section\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$22\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$26 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005111009,"name":"Clinical: Pharmacy","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4254906009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4149060009,"location":{"name":"Baltimore, Maryland"},"metadata":null,"id":4254906009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"259","title":"Phlebotomist - Clinical Research Assistant","company_name":"Headlands Research","first_published":"2026-05-21T11:11:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;167\u0026quot; data-end=\u0026quot;247\u0026quot;\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-exfc11cw_A\u0026quot;\u0026gt;📍\u0026amp;nbsp;\u0026lt;strong\u0026gt;Pikesville, MD\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-qFsrSOZK5Z\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong\u0026gt;PharmaSite Research\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;ql-block\u0026quot; data-block-id=\u0026quot;block-Ez0pTXSu9i\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong\u0026gt;Full-Time | Monday through Friday | 9:00am - 5:00pm\u0026lt;/strong\u0026gt;\u0026lt;/div\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;s6vv15\u0026quot; data-start=\u0026quot;249\u0026quot; data-end=\u0026quot;298\u0026quot;\u0026gt;Launch Your Career in Healthcare \u0026amp;amp; Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;268\u0026quot; data-end=\u0026quot;528\u0026quot;\u0026gt;Are you a recent graduate looking to gain hands-on experience in healthcare or clinical research? This is an exciting opportunity to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;530\u0026quot; data-end=\u0026quot;935\u0026quot;\u0026gt;As a\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;535\u0026quot; data-end=\u0026quot;566\u0026quot;\u0026gt;Clinical Research Assistant\u0026lt;/strong\u0026gt;, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you\u0026#39;re planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;299\u0026quot; data-end=\u0026quot;612\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;951\u0026quot; data-end=\u0026quot;954\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;xti9y5\u0026quot; data-start=\u0026quot;956\u0026quot; data-end=\u0026quot;976\u0026quot;\u0026gt;Responsibilities:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Study Preparation\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participant Care and Interaction\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with participant stipend tracking and processing.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Laboratory and Specimen Handling\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and file weekly temperature reports for laboratory systems.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data Entry and Management\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administrative and General Support\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings, study teleconferences, and trainings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with onsite or remote clinical research monitor visits.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1487\u0026quot; data-end=\u0026quot;1490\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1f5kc01\u0026quot; data-start=\u0026quot;1492\u0026quot; data-end=\u0026quot;1524\u0026quot;\u0026gt;What Makes You a Great Fit\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and ability to follow step-by-step procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work efficiently in a fast-paced environment with changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills and a professional, patient-focused demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable interacting with a diverse patient population\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive, dependable, and eager to learn new skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance multiple tasks and priorities throughout the day\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional, reliable, and eager to learn\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2035\u0026quot; data-end=\u0026quot;2038\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h3\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1qhx44\u0026quot; data-start=\u0026quot;2040\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Requirements:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2393\u0026quot;\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience as or certification/license as a CNA, Medical Assistant, Phlebotomist, or other direct-patient-care healthcare role required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with medical terminology and laboratory procedures helpful.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail, with the ability to collect, compile, and analyze patient data accurately.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal, communication (verbal and written), and customer service skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Easily able to learn new computer or website applications (i.e. Electronic Medical Records, Clinial Trial Management Systems, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to prioritize tasks, meet deadlines, and adapt to a fast-paced work environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-solving skills with a proactive and solution-oriented approach.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills with the proven ability to prioritize tasks and meet strict deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xrynm\u0026quot; data-start=\u0026quot;2061\u0026quot; data-end=\u0026quot;2100\u0026quot;\u0026gt;Phlebotomy training and experience heavily preferred; willingness to become fully trained required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2395\u0026quot; data-end=\u0026quot;2398\u0026quot;\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;iyhmpw\u0026quot; data-start=\u0026quot;2400\u0026quot; data-end=\u0026quot;2441\u0026quot;\u0026gt;Why This Role is a Great First Step\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;wylw1b\u0026quot; data-start=\u0026quot;3300\u0026quot; data-end=\u0026quot;3381\u0026quot;\u0026gt;Gain hands-on experience working directly with patients in a clinical setting\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;16gzdnb\u0026quot; data-start=\u0026quot;3382\u0026quot; data-end=\u0026quot;3458\u0026quot;\u0026gt;Learn the fundamentals of clinical research and how trials are conducted\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1o8ku67\u0026quot; data-start=\u0026quot;3459\u0026quot; data-end=\u0026quot;3542\u0026quot;\u0026gt;Build transferable skills for careers in healthcare, research, or biotechnology\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;4waw5a\u0026quot; data-start=\u0026quot;3543\u0026quot; data-end=\u0026quot;3623\u0026quot;\u0026gt;Work alongside experienced professionals who provide training and mentorship\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1on929o\u0026quot; data-start=\u0026quot;3624\u0026quot; data-end=\u0026quot;3726\u0026quot;\u0026gt;Create a strong foundation for advancement into roles like Clinical Research Coordinator or beyond\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;uvrqhh\u0026quot; data-start=\u0026quot;3727\u0026quot; data-end=\u0026quot;3813\u0026quot;\u0026gt;Make a meaningful impact by helping bring new treatments and therapies to patients\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2768\u0026quot; data-end=\u0026quot;2771\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2773\u0026quot; data-end=\u0026quot;2928\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;If you\u0026#39;re looking to turn your academic experience into a meaningful, patient-focused career, this is a powerful place to start.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4201773009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4117814009,"location":{"name":"Riverside, California"},"metadata":null,"id":4201773009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"202","title":"Phlebotomist/Lab Tech","company_name":"Headlands Research","first_published":"2026-03-30T09:50:56-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;The Laboratory Technician is a key member of the clinical research and laboratory operations team, responsible for performing a variety of technical and administrative tasks in support of clinical trials. This includes specimen collection, processing, documentation, and shipment in accordance with Good Clinical Practice (GCP), study protocols, and safety regulations. The technician will work with sensitive laboratory equipment, maintain a clean and organized lab environment, and assist with vital signs, ECGs, and data entry. A successful candidate will be detail-oriented, safety-conscious, and committed to supporting high-quality clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type: \u0026lt;/strong\u0026gt;\u0026amp;nbsp;Regular Full-time Employee\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026amp;nbsp; \u0026lt;/strong\u0026gt;$22 - $26/hr\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;Mondays through Fridays, 8:00am - 5:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Onsite in Riverside, CA (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Laboratory \u0026amp;amp; Clinical Procedures\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare lab kits for each subject based on study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ship biological specimens following IATA guidelines and protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain specimen logs, shipping records, temperature logs, and other documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean and sanitize lab equipment and work areas daily.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Data \u0026amp;amp; Documentation\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to and resolve electronic data queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify accuracy and completeness of data entries and study documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in quality control and assurance initiatives to ensure regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operational Support\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monitor and maintain inventory of lab kits and supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Order dry ice and other lab necessities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Destroy expired kits and log per protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation of study-specific training materials and lab manuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with study coordinators and medical staff to meet visit protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May assist with infusion monitoring under clinician supervision.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Requirements:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High School Diploma or GED required; Bachelor\u0026#39;s degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Phlebotomy certification or equivalent required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1 year of experience in a clinical lab setting required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Phase I-IV clinical trials and relevant regulatory environments (GCP, GLP, ICH) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle infectious and potentially hazardous materials safely.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physically able to lift up to 50 lbs and endure periods of standing/movement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, time management, and multitasking skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication; strong interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and as part of a cross-functional team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Customer-service mindset and high level of professionalism.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005110009,"name":"Clinical: Laboratory","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4169752009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4099146009,"location":{"name":"Wilmington, North Carolina"},"metadata":null,"id":4169752009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"169","title":"Phlebotomist/Lab Tech","company_name":"Headlands Research","first_published":"2026-03-04T09:09:02-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p data-start=\u0026quot;481\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;📍 \u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Wilmington, NC\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;500\u0026quot; data-end=\u0026quot;503\u0026quot;\u0026gt;🏥\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;506\u0026quot; data-end=\u0026quot;558\u0026quot;\u0026gt;Trial Management Associates\u0026lt;/strong\u0026gt;\u0026lt;br data-start=\u0026quot;558\u0026quot; data-end=\u0026quot;561\u0026quot;\u0026gt;🕒\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Full-Time | Monday through Friday\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;622\u0026quot; data-end=\u0026quot;677\u0026quot;\u0026gt;\u0026lt;em\u0026gt;Looking for more than just high-volume blood draws?\u0026lt;/em\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;678\u0026quot; data-end=\u0026quot;887\u0026quot;\u0026gt;If you’re a phlebotomist or lab technician who takes pride in precision, patient care, and doing things the \u0026lt;em data-start=\u0026quot;799\u0026quot; data-end=\u0026quot;806\u0026quot;\u0026gt;right\u0026lt;/em\u0026gt;\u0026amp;nbsp;way—not just the fast way—clinical research may be the next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;889\u0026quot; data-end=\u0026quot;1124\u0026quot;\u0026gt;At\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;892\u0026quot; data-end=\u0026quot;919\u0026quot;\u0026gt;Trial Management Associates\u0026lt;/strong\u0026gt;, our lab professionals work in a\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;953\u0026quot; data-end=\u0026quot;1005\u0026quot;\u0026gt;structured, calm, and purpose-driven environment\u0026lt;/strong\u0026gt;, supporting clinical trials that help advance new treatments for psychiatric, dementia, and memory-related conditions.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;889\u0026quot; data-end=\u0026quot;1124\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1126\u0026quot; data-end=\u0026quot;1129\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1131\u0026quot; data-end=\u0026quot;1184\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1134\u0026quot; data-end=\u0026quot;1184\u0026quot;\u0026gt;Why Lab Professionals Choose Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1187\u0026quot; data-end=\u0026quot;1266\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1187\u0026quot; data-end=\u0026quot;1219\u0026quot;\u0026gt;Predictable weekday schedule\u0026lt;/strong\u0026gt;\u0026amp;nbsp;(no nights, no weekends, no emergency draws)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1269\u0026quot; data-end=\u0026quot;1340\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1269\u0026quot; data-end=\u0026quot;1294\u0026quot;\u0026gt;More time and control\u0026lt;/strong\u0026gt;\u0026amp;nbsp;during patient visits and specimen handling\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1343\u0026quot; data-end=\u0026quot;1431\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1343\u0026quot; data-end=\u0026quot;1367\u0026quot;\u0026gt;Specialized lab work\u0026lt;/strong\u0026gt;\u0026amp;nbsp;beyond routine phlebotomy (processing, PK handling, shipping)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1434\u0026quot; data-end=\u0026quot;1497\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1434\u0026quot; data-end=\u0026quot;1466\u0026quot;\u0026gt;Smaller, collaborative teams\u0026lt;/strong\u0026gt;\u0026amp;nbsp;where your role is respected\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1500\u0026quot; data-end=\u0026quot;1578\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1500\u0026quot; data-end=\u0026quot;1522\u0026quot;\u0026gt;Meaningful purpose\u0026lt;/strong\u0026gt;—your work directly supports future medical treatments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;1652\u0026quot; data-end=\u0026quot;1826\u0026quot;\u0026gt;This role is ideal for lab professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;1703\u0026quot; data-end=\u0026quot;1746\u0026quot;\u0026gt;accuracy, organization, and consistency\u0026lt;/strong\u0026gt;, and who want to grow their skills beyond traditional lab or hospital settings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2511\u0026quot; data-end=\u0026quot;2514\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2516\u0026quot; data-end=\u0026quot;2531\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2519\u0026quot; data-end=\u0026quot;2531\u0026quot;\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;2532\u0026quot; data-end=\u0026quot;2801\u0026quot;\u0026gt;The Phlebotomist/Lab Tech is a key member of the clinical research team, supporting studies through \u0026lt;strong data-start=\u0026quot;2647\u0026quot; data-end=\u0026quot;2711\u0026quot;\u0026gt;specimen collection, processing, documentation, and shipment\u0026lt;/strong\u0026gt;\u0026amp;nbsp;in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2803\u0026quot; data-end=\u0026quot;2987\u0026quot;\u0026gt;You’ll work in a controlled clinical research environment with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2866\u0026quot; data-end=\u0026quot;2938\u0026quot;\u0026gt;scheduled visits, detailed protocols, and strong operational support\u0026lt;/strong\u0026gt;, allowing you to focus on quality and precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2803\u0026quot; data-end=\u0026quot;2987\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4883\u0026quot; data-end=\u0026quot;4886\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4888\u0026quot; data-end=\u0026quot;4919\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4891\u0026quot; data-end=\u0026quot;4919\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4922\u0026quot; data-end=\u0026quot;4976\u0026quot;\u0026gt;Lab professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4950\u0026quot; data-end=\u0026quot;4974\u0026quot;\u0026gt;precision over speed\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4979\u0026quot; data-end=\u0026quot;5037\u0026quot;\u0026gt;Phlebotomists looking for\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5005\u0026quot; data-end=\u0026quot;5035\u0026quot;\u0026gt;predictability and balance\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5040\u0026quot; data-end=\u0026quot;5102\u0026quot;\u0026gt;Candidates curious about clinical research and career growth\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;5105\u0026quot; data-end=\u0026quot;5181\u0026quot;\u0026gt;Team players who take pride in quality, compliance, and patient experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5183\u0026quot; data-end=\u0026quot;5186\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare lab kits for each subject based on study protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ship biological specimens following IATA guidelines and protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain specimen logs, shipping records, temperature logs, and other documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clean and sanitize lab equipment and work areas daily.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to and resolve electronic data queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify accuracy and completeness of data entries and study documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in quality control and assurance initiatives to ensure regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and maintain inventory of lab kits and supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Order dry ice and other lab necessities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Destroy expired kits and log per protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation of study-specific training materials and lab manuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with study coordinators and medical staff to meet visit protocol requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May assist with infusion monitoring under clinician supervision.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Must be certified in phlebotomy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous healthcare experience preferred; direct patient care experience a huge bonus!\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience in clinical research is a huge plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be comfortable with performing Research Assistant tasks when the lab is slow.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle potentially hazardous materials safely.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, time management, and multitasking skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication; strong interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and as part of a cross-functional team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Customer-service mindset and high level of professionalism.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$18\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$22 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005110009,"name":"Clinical: Laboratory","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004754009,"name":"North Carolina - Wilmington","location":"Wilmington, North Carolina, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4204305009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4119300009,"location":{"name":"Chesterfield, Missouri"},"metadata":null,"id":4204305009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"207","title":"Physician Assistant - Clinical Research","company_name":"Headlands Research","first_published":"2026-03-31T15:14:55-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us - it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced Physician Assistant or Nurse Practitioner to help us grow our clinical research site located in the Greater St. Louis Area. You will help the site conduct clinical research trials involving gastroenterology, neurology, vaccines, and general internal medicine.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Professionals (CRP) is a dedicated research center that provides a network of providers who work collaboratively in conducting clinical research trials. The site’s team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Full-time Regular Employee\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Competitive and dependent upon years of experience as an Investigator in clinical research.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Onsite in Chesterfield, MO (no opportunities for remote or hybrid)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am-5:00pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure the safety and welfare of each study subject\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have in-depth knowledge of all research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct medical history interviews and physical examinations throughout the subject’s study participation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review EKG’s and lab results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical care as needed during a subject’s participation in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide home based on-call availability per standard policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend Investigator Meetings on behalf of Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent professional communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Friendly and outgoing demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must demonstrate a passion for direct patient interaction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an PA or NP in the state of Missouri required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience within the clinical research industry highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4257215009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4144099009,"location":{"name":"Plymouth, Massachusetts"},"metadata":null,"id":4257215009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"252","title":"Physician Assistant - Plymouth, MA - Clinical Research","company_name":"Headlands Research","first_published":"2026-05-21T17:42:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1tw2tfc\u0026quot; data-start=\u0026quot;0\u0026quot; data-end=\u0026quot;43\u0026quot;\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;45\u0026quot; data-end=\u0026quot;458\u0026quot;\u0026gt;At \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;48\u0026quot; data-end=\u0026quot;122\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt;, diversity is not just a goal — it is foundational to how we advance medicine. We are committed to improving representation in clinical research and ensuring patients from all backgrounds have access to innovative treatment opportunities. From the patients we serve to the teams we build, inclusivity is embedded into everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;618\u0026quot; data-end=\u0026quot;652\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;19cyuv5\u0026quot; data-start=\u0026quot;654\u0026quot; data-end=\u0026quot;714\u0026quot;\u0026gt;Make a Meaningful Impact in Dementia \u0026amp;amp; Neurology Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;1080\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearchema.com/?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;716\u0026quot; data-end=\u0026quot;816\u0026quot;\u0026gt;Headlands Research Eastern Massachusetts\u0026lt;/a\u0026gt;, in partnership with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;838\u0026quot; data-end=\u0026quot;918\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt;, is seeking an experienced Nurse Practitioner or Physician Assistant to join our growing clinical research team as a Sub-Investigator in Plymouth, Massachusetts.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1082\u0026quot; data-end=\u0026quot;1383\u0026quot;\u0026gt;This role is ideal for an advanced provider who is passionate about caring for adult and geriatric patients - particularly those affected by Alzheimer’s disease, dementia, and other neurological conditions - and who wants to play a direct role in advancing future treatments through clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1385\u0026quot; data-end=\u0026quot;1615\u0026quot;\u0026gt;We are especially interested in connecting with providers who live within a commutable distance to Plymouth and who value building strong relationships with patients and caregivers in a collaborative, patient-centered environment.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;ca302g\u0026quot; data-start=\u0026quot;1622\u0026quot; data-end=\u0026quot;1637\u0026quot;\u0026gt;Why Join Us?\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r7878a\u0026quot; data-start=\u0026quot;1639\u0026quot; data-end=\u0026quot;1679\u0026quot;\u0026gt;Meaningful Work in Dementia Research\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1680\u0026quot; data-end=\u0026quot;1847\u0026quot;\u0026gt;Help bring innovative therapies to patients living with Alzheimer’s disease and related dementias while supporting families navigating complex neurological conditions.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;80ghtc\u0026quot; data-start=\u0026quot;1849\u0026quot; data-end=\u0026quot;1896\u0026quot;\u0026gt;Collaborative Neurology-Focused Environment\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;1897\u0026quot; data-end=\u0026quot;2078\u0026quot;\u0026gt;Work alongside experienced neurologists, clinical research coordinators, raters, and patient recruitment specialists as part of both Headlands Research and Seacoast Neurology Group.\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;107ic8x\u0026quot; data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2254\u0026quot;\u0026gt;Supportive, High-Performing Culture\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;2255\u0026quot; data-end=\u0026quot;2480\u0026quot;\u0026gt;Our teams value professionalism, accountability, compassion, and collaboration. You will be supported by experienced research staff while having the opportunity to grow your clinical research experience and leadership skills.\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;484\u0026quot; data-end=\u0026quot;500\u0026quot;\u0026gt;Location: \u0026amp;nbsp; \u0026lt;/strong\u0026gt;Onsite in Plymouth, Massachusetts (no remote or hybrid opportunities)\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Schedule:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Full-Time | Monday through Friday\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;643\u0026quot; data-end=\u0026quot;825\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;620\u0026quot;\u0026gt;Pay:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;$120,000 - 140,000/yr (dependent upon years of experience, certifications, and education)\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;r8dte7\u0026quot; data-start=\u0026quot;2857\u0026quot; data-end=\u0026quot;2876\u0026quot;\u0026gt;Responsibilities:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;6hqsmy\u0026quot; data-start=\u0026quot;2878\u0026quot; data-end=\u0026quot;2940\u0026quot;\u0026gt;Ensure the safety and welfare of clinical trial participants\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;tkipd6\u0026quot; data-start=\u0026quot;2941\u0026quot; data-end=\u0026quot;3000\u0026quot;\u0026gt;Conduct medical history reviews and physical examinations\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1arrgwj\u0026quot; data-start=\u0026quot;3001\u0026quot; data-end=\u0026quot;3091\u0026quot;\u0026gt;Evaluate potential study participants according to protocol inclusion/exclusion criteria\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;c50yt0\u0026quot; data-start=\u0026quot;3092\u0026quot; data-end=\u0026quot;3157\u0026quot;\u0026gt;Review EKGs, laboratory results, and other clinical assessments\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;14sy18i\u0026quot; data-start=\u0026quot;3158\u0026quot; data-end=\u0026quot;3225\u0026quot;\u0026gt;Provide medical oversight and care throughout study participation\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1xox3k8\u0026quot; data-start=\u0026quot;3226\u0026quot; data-end=\u0026quot;3324\u0026quot;\u0026gt;Develop strong rapport with dementia patients and caregivers through compassionate communication\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1914vgm\u0026quot; data-start=\u0026quot;3325\u0026quot; data-end=\u0026quot;3416\u0026quot;\u0026gt;Collaborate closely with neurologists, research coordinators, and sponsor representatives\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;8mm6up\u0026quot; data-start=\u0026quot;3417\u0026quot; data-end=\u0026quot;3477\u0026quot;\u0026gt;Maintain in-depth knowledge of assigned research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;9f28cy\u0026quot; data-start=\u0026quot;3478\u0026quot; data-end=\u0026quot;3558\u0026quot;\u0026gt;Attend Investigator Meetings on behalf of the Principal Investigator as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1wfhkz3\u0026quot; data-start=\u0026quot;3559\u0026quot; data-end=\u0026quot;3621\u0026quot;\u0026gt;Support high-quality data collection and protocol compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;18ypsib\u0026quot; data-start=\u0026quot;3622\u0026quot; data-end=\u0026quot;3710\u0026quot;\u0026gt;Demonstrate professionalism, accountability, and strong patient-centered communication\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h3 data-section-id=\u0026quot;1fm6vrb\u0026quot; data-start=\u0026quot;3717\u0026quot; data-end=\u0026quot;3734\u0026quot;\u0026gt;Requirements:\u0026lt;/h3\u0026gt;\n\u0026lt;ul data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;nuseyd\u0026quot; data-start=\u0026quot;3736\u0026quot; data-end=\u0026quot;3835\u0026quot;\u0026gt;Minimum of 2 years of experience as a licensed Nurse Practitioner or Physician Assistant preferred; willing to consider new graduates\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;1io90kj\u0026quot; data-start=\u0026quot;3836\u0026quot; data-end=\u0026quot;3918\u0026quot;\u0026gt;Current and unencumbered NP or PA license in the state of Massachusetts required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;vmz64g\u0026quot; data-start=\u0026quot;3919\u0026quot; data-end=\u0026quot;3993\u0026quot;\u0026gt;Experience working with adult and geriatric patient populations required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;j5uwn4\u0026quot; data-start=\u0026quot;3994\u0026quot; data-end=\u0026quot;4159\u0026quot;\u0026gt;Prior experience caring for patients with dementia, Alzheimer’s disease, neurology, geriatrics, psychiatry, primary care, or related specialties strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;ehkut2\u0026quot; data-start=\u0026quot;4160\u0026quot; data-end=\u0026quot;4218\u0026quot;\u0026gt;Clinical research experience preferred, but not required\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;156lb62\u0026quot; data-start=\u0026quot;4219\u0026quot; data-end=\u0026quot;4342\u0026quot;\u0026gt;Strong interpersonal skills with the ability to communicate effectively with cognitively impaired patients and caregivers\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;5sxdnd\u0026quot; data-start=\u0026quot;4343\u0026quot; data-end=\u0026quot;4393\u0026quot;\u0026gt;Highly organized with strong attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;yt3tga\u0026quot; data-start=\u0026quot;4394\u0026quot; data-end=\u0026quot;4448\u0026quot;\u0026gt;Professional, dependable, and collaborative demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;41qls8\u0026quot; data-start=\u0026quot;4449\u0026quot; data-end=\u0026quot;4520\u0026quot;\u0026gt;Passion for direct patient interaction and advancing medical research\u0026lt;/li\u0026gt;\n\u0026lt;li data-section-id=\u0026quot;lm26i9\u0026quot; data-start=\u0026quot;4521\u0026quot; data-end=\u0026quot;4592\u0026quot;\u0026gt;Ability to thrive in a fast-paced, team-oriented clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/h2\u0026gt;\n\u0026lt;h2 data-section-id=\u0026quot;9k4pt9\u0026quot; data-start=\u0026quot;4599\u0026quot; data-end=\u0026quot;4626\u0026quot;\u0026gt;About Headlands Research\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;5037\u0026quot;\u0026gt;\u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://headlandsresearch.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;4628\u0026quot; data-end=\u0026quot;4702\u0026quot;\u0026gt;Headlands Research\u0026lt;/a\u0026gt; is a leading integrated clinical trial site network with a mission to improve lives by advancing innovative medical therapies. Our sites partner with sponsors and CROs to conduct high-quality clinical trials across a variety of therapeutic areas while delivering exceptional patient care and operational excellence.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5039\u0026quot; data-end=\u0026quot;5273\u0026quot; data-is-last-node=\u0026quot;\u0026quot; data-is-only-node=\u0026quot;\u0026quot;\u0026gt;At our Eastern Massachusetts site, we are proud to partner closely with \u0026lt;a class=\u0026quot;decorated-link\u0026quot; href=\u0026quot;https://seacoastneurology.com?utm_source=chatgpt.com\u0026quot; target=\u0026quot;_new\u0026quot; data-start=\u0026quot;5111\u0026quot; data-end=\u0026quot;5191\u0026quot;\u0026gt;Seacoast Neurology Group\u0026lt;/a\u0026gt; to advance neurological and dementia-focused research within the local community.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005105009,"name":"Clinical: Advanced Providers","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4245260009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4143177009,"location":{"name":"San Diego, California"},"metadata":null,"id":4245260009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"249","title":"Physician - Clinical Research","company_name":"Headlands Research","first_published":"2026-05-22T16:10:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Company\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in psychiatry/neurology, internal medicine, and women’s health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;full-time\u0026lt;/strong\u0026gt; (30-32 hours per week) physician to help us grow our clinical research site at Artemis Institute for Clinical Research in \u0026lt;strong\u0026gt;San Diego\u0026lt;/strong\u0026gt;; primarily seeking physicians with previous experience serving as a Principal Investigator (PI) on vaccine, metabolic, and other pharmaceutical clinical trials. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Artemis Institute for Clinical Research San Diego, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Eligible for or active unencumbered license to practice as an MD or DO within the state of California required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;IV experience strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$130\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011186009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4008997009,"location":{"name":"Little Rock, AR"},"metadata":null,"id":4011186009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1796","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:10:58-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Little Rock\u0026amp;nbsp;\u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of Arkansas required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011185009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4008996009,"location":{"name":"Albuquerque, New Mexico"},"metadata":null,"id":4011185009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1795","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:10:35-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Albuquerque \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of New Mexico required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011194009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009004009,"location":{"name":"Denver, CO"},"metadata":null,"id":4011194009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1898","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2026-03-06T09:31:49-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Denver \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of Colorado required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011189009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009000009,"location":{"name":"Buffalo, NY"},"metadata":null,"id":4011189009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1893","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2026-03-04T11:55:17-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Buffalo \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of New York required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011190009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009001009,"location":{"name":"Charlotte, NC"},"metadata":null,"id":4011190009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1899","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2026-03-06T09:31:41-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Charlotte \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of North Carolina required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011188009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4008999009,"location":{"name":"Milwaukee, WI"},"metadata":null,"id":4011188009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1892","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:12:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Milwaukee \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of Wisconsin required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; 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data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011195009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009005009,"location":{"name":"Colorado Springs, CO"},"metadata":null,"id":4011195009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1886","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:11:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Colorado Springs \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of Colorado required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; 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data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011197009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009007009,"location":{"name":"Las Cruces, NM"},"metadata":null,"id":4011197009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1861","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:11:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Las Cruces \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of New Mexico required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4011198009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4009008009,"location":{"name":"Memphis, TN"},"metadata":null,"id":4011198009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"2025-1797","title":"Physician - Clinical Trials - MD/DO","company_name":"Headlands Research","first_published":"2025-09-17T09:11:14-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Join Us in Improving Lives through Clinical Research\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Headlands Research, we\u0026#39;re not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we\u0026#39;ve rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced \u0026lt;strong\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; to help us grow a new clinical research site in the \u0026lt;strong\u0026gt;Memphis \u0026lt;/strong\u0026gt;area. Whether you\u0026#39;re a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We\u0026#39;re flexible—we\u0026#39;re open to part-time or full-time commitments with flexible schedules.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Unlimited Potential\u0026lt;/strong\u0026gt;: The sky\u0026#39;s the limit. We\u0026#39;re open to up to 40 hours per week, allowing you to maximize your impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Active and unencumbered license to practice as an MD or DO within the state of Tennessee required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4108146009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4073887009,"location":{"name":"Atlanta, Georgia; Baltimore, Maryland; Brownsville, Texas; Chesterfield, Missouri; Detroit, Michigan; El Paso, Texas; Escondido, California; Kelowna, British Columbia; Lake Worth, Florida; Maplewood, Minnesota; Myrtle Beach, South Carolina; Orlando, Florida; Plymouth, Massachusetts; Portland, Oregon; Richmond, British Columbia; Riverside, California; Rolling Hills Estates, California; San Diego, California; San Juan, Puerto Rico; Scottsdale, Arizona; Springfield, Missouri; Toronto, Ontario; Wilmington, North Carolina"},"metadata":null,"id":4108146009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"126","title":"Physician Investigator Opportunities – Multiple Locations Nationwide","company_name":"Headlands Research","first_published":"2026-01-23T13:22:14-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;564\u0026quot; data-end=\u0026quot;588\u0026quot;\u0026gt;About the Opportunity\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;590\u0026quot; data-end=\u0026quot;1059\u0026quot;\u0026gt;We are always interested in connecting with \u0026lt;strong data-start=\u0026quot;634\u0026quot; data-end=\u0026quot;725\u0026quot;\u0026gt;physicians who are curious about, experienced in, or passionate about clinical research\u0026lt;/strong\u0026gt;. This general interest posting is designed for physicians who may not see a current opening that perfectly aligns with their location or specialty—but who would like to be considered for \u0026lt;strong data-start=\u0026quot;913\u0026quot; data-end=\u0026quot;993\u0026quot;\u0026gt;future Investigator, Sub-Investigator, or Physician leadership opportunities\u0026lt;/strong\u0026gt; across our growing network of clinical research sites nationwide.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1061\u0026quot; data-end=\u0026quot;1242\u0026quot;\u0026gt;Our physicians play a critical role in advancing innovative therapies, improving patient access to clinical trials, and shaping high-quality, patient-centered research environments.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1244\u0026quot; data-end=\u0026quot;1247\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1249\u0026quot; data-end=\u0026quot;1294\u0026quot;\u0026gt;Our Process\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1339\u0026quot; data-end=\u0026quot;1755\u0026quot;\u0026gt;When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;1448\u0026quot; data-end=\u0026quot;1496\u0026quot;\u0026gt;current and upcoming physician opportunities\u0026lt;/strong\u0026gt;. As new roles open, we proactively match candidates based on \u0026lt;strong data-start=\u0026quot;1558\u0026quot; data-end=\u0026quot;1644\u0026quot;\u0026gt;location preference, specialty, prior research experience, and leadership interest\u0026lt;/strong\u0026gt;. If a role aligns with your background and goals, a recruiter will reach out directly to begin a conversation.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1757\u0026quot; data-end=\u0026quot;1760\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1762\u0026quot; data-end=\u0026quot;1810\u0026quot;\u0026gt;What Physician Roles Look Like at Our Company\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1812\u0026quot; data-end=\u0026quot;1875\u0026quot;\u0026gt;Physicians may serve as \u0026lt;strong data-start=\u0026quot;1879\u0026quot; data-end=\u0026quot;1925\u0026quot;\u0026gt;Principal Investigator or Sub-Investigator\u0026lt;/strong\u0026gt; on Phase II–IV clinical trials. Roles may be \u0026lt;strong data-start=\u0026quot;2249\u0026quot; data-end=\u0026quot;2275\u0026quot;\u0026gt;part-time or full-time\u0026lt;/strong\u0026gt;, and responsibilities vary based on experience, interest, and site needs.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2351\u0026quot; data-end=\u0026quot;2354\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2356\u0026quot; data-end=\u0026quot;2380\u0026quot;\u0026gt;Who We’re Looking For\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;2382\u0026quot; data-end=\u0026quot;2428\u0026quot;\u0026gt;We welcome interest from physicians who bring:\u0026lt;/p\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2430\u0026quot; data-end=\u0026quot;2784\u0026quot;\u0026gt;\n\u0026lt;li data-start=\u0026quot;2430\u0026quot; data-end=\u0026quot;2479\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2432\u0026quot; data-end=\u0026quot;2479\u0026quot;\u0026gt;An MD or DO (board-certified or board-eligible required)\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2480\u0026quot; data-end=\u0026quot;2567\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2482\u0026quot; data-end=\u0026quot;2567\u0026quot;\u0026gt;An interest in clinical research, increasing patient access to trials, or innovation in medicine\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2568\u0026quot; data-end=\u0026quot;2627\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2570\u0026quot; data-end=\u0026quot;2627\u0026quot;\u0026gt;Strong clinical judgment and commitment to patient safety\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2628\u0026quot; data-end=\u0026quot;2711\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2630\u0026quot; data-end=\u0026quot;2711\u0026quot;\u0026gt;Clear communication skills and comfort collaborating with multidisciplinary teams\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2712\u0026quot; data-end=\u0026quot;2784\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2714\u0026quot; data-end=\u0026quot;2784\u0026quot;\u0026gt;Prior research experience is valued but \u0026lt;strong data-start=\u0026quot;2754\u0026quot; data-end=\u0026quot;2770\u0026quot;\u0026gt;not required\u0026lt;/strong\u0026gt; for all roles\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2786\u0026quot; data-end=\u0026quot;2854\u0026quot;\u0026gt;Physicians from a wide range of specialties are encouraged to apply.\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2856\u0026quot; data-end=\u0026quot;2859\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2861\u0026quot; data-end=\u0026quot;2911\u0026quot;\u0026gt;Why Physicians Choose Clinical Research with Us\u0026lt;/h2\u0026gt;\n\u0026lt;ul data-start=\u0026quot;2913\u0026quot; data-end=\u0026quot;3261\u0026quot;\u0026gt;\n\u0026lt;li data-start=\u0026quot;2913\u0026quot; data-end=\u0026quot;2980\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2915\u0026quot; data-end=\u0026quot;2980\u0026quot;\u0026gt;Opportunity to \u0026lt;strong data-start=\u0026quot;2930\u0026quot; data-end=\u0026quot;2980\u0026quot;\u0026gt;expand your impact beyond traditional practice\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2981\u0026quot; data-end=\u0026quot;3033\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;2983\u0026quot; data-end=\u0026quot;3033\u0026quot;\u0026gt;Meaningful involvement in advancing new treatments\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3034\u0026quot; data-end=\u0026quot;3114\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;3036\u0026quot; data-end=\u0026quot;3114\u0026quot;\u0026gt;Supportive infrastructure, research operations teams, and regulatory expertise\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3115\u0026quot; data-end=\u0026quot;3191\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;3117\u0026quot; data-end=\u0026quot;3191\u0026quot;\u0026gt;The chance to grow into \u0026lt;strong data-start=\u0026quot;3141\u0026quot; data-end=\u0026quot;3181\u0026quot;\u0026gt;leadership roles\u0026lt;/strong\u0026gt; over time\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;3192\u0026quot; data-end=\u0026quot;3261\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;3194\u0026quot; data-end=\u0026quot;3261\u0026quot;\u0026gt;Alignment with a mission-driven, patient-first research environment\u0026lt;/p\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;hr data-start=\u0026quot;3263\u0026quot; data-end=\u0026quot;3266\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;3268\u0026quot; data-end=\u0026quot;3303\u0026quot;\u0026gt;Ready to Start the Conversation?\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;3305\u0026quot; data-end=\u0026quot;3538\u0026quot;\u0026gt;If you’re interested in learning more about physician opportunities within clinical research—now or in the future—we invite you to apply here. Our Talent Acquisition team looks forward to connecting when the right opportunity arises.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004740009,"name":"Arizona - Scottsdale","location":"Scottsdale, Arizona, United States","child_ids":[],"parent_id":4004735009},{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004739009,"name":"California - Rolling Hills Estates/Palos Verdes","location":"Rolling Hills Estates, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004737009,"name":"California - San Diego","location":"San Diego, California, United States","child_ids":[],"parent_id":4004735009},{"id":4004756009,"name":"Canada - Kelowna, BC","location":"Kelowna, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004755009,"name":"Canada - Richmond, BC","location":"Richmond, British Columbia, Canada","child_ids":[],"parent_id":4004735009},{"id":4004757009,"name":"Canada - Toronto, ON","location":"Toronto, Ontario, Canada","child_ids":[],"parent_id":4004734009},{"id":4004732009,"name":"Corporate","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":null},{"id":4004750009,"name":"Florida - Lake Worth","location":"Lake Worth, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004751009,"name":"Florida - Orlando","location":"Orlando, Florida, United States","child_ids":[],"parent_id":4004733009},{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009},{"id":4004752009,"name":"Maryland - Baltimore","location":"Pikesville, Maryland, United States","child_ids":[],"parent_id":4004733009},{"id":4004749009,"name":"Massachusetts - Boston","location":"Plymouth, Massachusetts, United States","child_ids":[],"parent_id":4004733009},{"id":4004745009,"name":"Michigan - Detroit","location":"Southfield, Michigan, United States","child_ids":[],"parent_id":4004734009},{"id":4004747009,"name":"Minnesota - Twin Cities","location":null,"child_ids":[],"parent_id":4004734009},{"id":4004744009,"name":"Missouri - Springfield","location":"Springfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009},{"id":4004754009,"name":"North Carolina - Wilmington","location":"Wilmington, North Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004741009,"name":"Oregon - Portland","location":"Portland, Oregon, United States","child_ids":[],"parent_id":4004735009},{"id":4007276009,"name":"Puerto Rico - San Juan","location":"San Juan, Puerto Rico","child_ids":[],"parent_id":4004733009},{"id":4004753009,"name":"South Carolina - Myrtle Beach","location":"Myrtle Beach, South Carolina, United States","child_ids":[],"parent_id":4004733009},{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009},{"id":4004746009,"name":"Texas - El Paso","location":"El Paso, Texas, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4205046009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4119794009,"location":{"name":"Atlanta, Georgia"},"metadata":null,"id":4205046009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"210","title":"Physician, MD/DO - Clinical Research ","company_name":"Headlands Research","first_published":"2026-04-01T15:50:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Company\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Atlanta (CRA), located in Stockbridge, Georgia, is a leading multi-specialty research center with a long-standing reputation for excellence. The site has delivered more than 300 clinical trials across a wide range of therapeutic areas, including addiction, dermatology, infectious diseases, and more. Known for exceptional recruitment performance, CRA consistently achieves efficient operations and reliable results. With its strong community presence and commitment to advancing medical innovation, CRA continues to contribute to the development of new therapies that improve patient health and outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference?\u0026amp;nbsp;With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an MD or DO within the state of Georgia required (or eligible for).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4117574009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4035820009,"location":{"name":"Detroit, Michigan"},"metadata":null,"id":4117574009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"69","title":"PRN/Per-Diem Physician, MD/DO","company_name":"Headlands Research","first_published":"2026-02-04T15:34:48-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Championing Diversity in Clinical Trials\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Diversity isn\u0026#39;t just a checkbox for us—it\u0026#39;s central to our mission. We\u0026#39;re committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role of a Lifetime\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Are you ready to make a difference? We\u0026#39;re seeking an experienced physician principal- or sub-investigator to help us grow our clinical research site at Headlands Research Detroit in Southfield, Michigan on a PRN or Per-Diem basis (also open to 1099 independent contractors).\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why Join Us?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Flexible Schedule\u0026lt;/strong\u0026gt;: Work on your terms, with a schedule that fits your life.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Dynamic Team Environment\u0026lt;/strong\u0026gt;: You\u0026#39;ll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you\u0026#39;ll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Obtain IRB approval for study initiation and any protocol modifications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee subject safety, trial conduct compliance, and the informed consent process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide ongoing training and support to research staff.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current and unencumbered license to practice as an MD or DO within the state of Michigan required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be board-certified or board-eligible.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005104009,"name":"Clinical: Physicians","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004745009,"name":"Michigan - Detroit","location":"Southfield, Michigan, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4271697009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4158423009,"location":{"name":"Escondido, California"},"metadata":null,"id":4271697009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"273","title":"PRN/Per-Diem Research Nurse (LVN)","company_name":"Headlands Research","first_published":"2026-06-02T15:48:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;OVERVIEW / POSITION DESCRIPTION\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The AMCR Institute is a cutting-edge research institute specializing in the execution of Phase I-IV diabetes device and biopharmaceutical trials. Eligible subjects are offered the latest treatment options carried out under the strict guidelines from the Food and Drug Administration (FDA). Research subjects (Volunteers) become the most critical link in a chain of research and testing to develop breakthrough treatments for a broad range of health problems including Type 1 and Type 2 Diabetes. At all times the safety and confidentiality are guarded with the utmost concern.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a member of AMCR Institute, you will contribute to the development of novel therapies and supportive technology for people with diabetes and be part of the discovery of new treatments.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Research Nurse (RN) is a licensed clinical professional working with and under the direction of the Principal Investigator, Assistant Director, Lead Research Nurse, and in close conjunction with the Clinical Project Manager on early or late phase clinical trials related to the treatment of diabetes. The Clinical Research Nurse is an integral member of the clinical trial team and assumes responsibility and accountability for the direct research care of a group of research subjects during a designated time frame. The Clinical Research Nurse is responsible for assuring compliance with the Federal and State regulations relating to research and the study protocol requirements.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MATERIALS AND EQUIPMENT DIRECTLY USED \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt; Phlebotomy and IV supplies including infusion pumps\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Office equipment such as personal computer, printer and copier, telephone, fax\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Diabetes-related medical devices (e.g. glucometer, insulin delivery devices, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;INTERRELATIONSHIPS \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physicians, Nurse Practitioners, Physician Assistants, Nurses, Research Staff, Research Subjects, and Clinical Office and Administrative Staff\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp; \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;DUTIES AND RESPONSIBILITIES\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Research / Regulatory:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Contributes to data collection by adhering to “Good Documentation Practices”\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Documents in detail the data obtained following AMCR Institute’s Standard Operating Procedure (SOP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competently recognizes signs and symptoms of Hypoglycemia, Hyperglycemia, and Ketosis and alerts the lead coordinator and clinician.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of research protocol to understand the science behind the study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists research staff in specimen processing: spinning, pipetting, and analyzing using the YSI glucose instrument.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Discharge research subject upon completion of in-clinic visit following the “Glycemic Discharge Protocol for AMCR Institute”.\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Clinical:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Conducts a centered research subject assessment focusing on safety and venous access placement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, identifies the largest accessible vein and starts intravenous placement (IV) on adults and pediatric research subjects. Number of IV lines depending on the research design. May place two (2) IV lines on the same arm and/or another line on the opposite arm.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, changes IV bags PRN and adjust infusion pumps flow rate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Employs strategies in maintaining subject’s safety: monitoring heating pad temperature, awareness of blood glucose levels, phlebitis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administers research drugs and/or medications as ordered by a clinician.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, assists research staff in blood drawing using a 3-way stopcock method.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists research staff with performing vital signs and EKG tracings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides the tools and necessary support to subjects in learning their diabetes management responsibilities in accordance with the protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides nursing support to staff regarding diabetes issues as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organizes and prioritizes workload to effectively accomplish goals. \u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Communicates clearly and effectively with clinicians, nursing and research staff, and research subjects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Check-in and report with the Lead Research Coordinator and/or RN at the start and end of each shift and provide a complete outgoing report.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sign / initial / and date all documents that were worked on during shift prior to leaving.\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;SCHEDULE\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Shift availability varies depending upon the type and number of active research protocols being executed. Shift may range from 4 to 12 hours. Some flexibility may be possible depending upon the protocol.\u0026amp;nbsp;RNs are strongly encouraged to attend monthly meetings led by the Lead Research Nurse. These meetings may include protocol and skills training, updates, and other topics as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$35\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$40 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005108009,"name":"Clinical: Nurses \u0026 Infusionists","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4271679009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4158423009,"location":{"name":"Escondido, California"},"metadata":null,"id":4271679009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"273","title":"PRN/Per-Diem Research Nurse (RN)","company_name":"Headlands Research","first_published":"2026-06-02T15:48:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;OVERVIEW / POSITION DESCRIPTION\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The AMCR Institute is a cutting-edge research institute specializing in the execution of Phase I-IV diabetes device and biopharmaceutical trials. Eligible subjects are offered the latest treatment options carried out under the strict guidelines from the Food and Drug Administration (FDA). Research subjects (Volunteers) become the most critical link in a chain of research and testing to develop breakthrough treatments for a broad range of health problems including Type 1 and Type 2 Diabetes. At all times the safety and confidentiality are guarded with the utmost concern.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a member of AMCR Institute, you will contribute to the development of novel therapies and supportive technology for people with diabetes and be part of the discovery of new treatments.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Research Nurse (RN) is a licensed clinical professional working with and under the direction of the Principal Investigator, Assistant Director, Lead Research Nurse, and in close conjunction with the Clinical Project Manager on early or late phase clinical trials related to the treatment of diabetes. The Clinical Research Nurse is an integral member of the clinical trial team and assumes responsibility and accountability for the direct research care of a group of research subjects during a designated time frame. The Clinical Research Nurse is responsible for assuring compliance with the Federal and State regulations relating to research and the study protocol requirements.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MATERIALS AND EQUIPMENT DIRECTLY USED \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt; Phlebotomy and IV supplies including infusion pumps\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Office equipment such as personal computer, printer and copier, telephone, fax\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Diabetes-related medical devices (e.g. glucometer, insulin delivery devices, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;INTERRELATIONSHIPS \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physicians, Nurse Practitioners, Physician Assistants, Nurses, Research Staff, Research Subjects, and Clinical Office and Administrative Staff\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp; \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;DUTIES AND RESPONSIBILITIES\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Research / Regulatory:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Contributes to data collection by adhering to “Good Documentation Practices”\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Documents in detail the data obtained following AMCR Institute’s Standard Operating Procedure (SOP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competently recognizes signs and symptoms of Hypoglycemia, Hyperglycemia, and Ketosis and alerts the lead coordinator and clinician.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of research protocol to understand the science behind the study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists research staff in specimen processing: spinning, pipetting, and analyzing using the YSI glucose instrument.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Discharge research subject upon completion of in-clinic visit following the “Glycemic Discharge Protocol for AMCR Institute”.\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Clinical:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Conducts a centered research subject assessment focusing on safety and venous access placement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, identifies the largest accessible vein and starts intravenous placement (IV) on adults and pediatric research subjects. Number of IV lines depending on the research design. May place two (2) IV lines on the same arm and/or another line on the opposite arm.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, changes IV bags PRN and adjust infusion pumps flow rate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Employs strategies in maintaining subject’s safety: monitoring heating pad temperature, awareness of blood glucose levels, phlebitis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administers research drugs and/or medications as ordered by a clinician.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Using aseptic technique, assists research staff in blood drawing using a 3-way stopcock method.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists research staff with performing vital signs and EKG tracings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides the tools and necessary support to subjects in learning their diabetes management responsibilities in accordance with the protocol.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides nursing support to staff regarding diabetes issues as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organizes and prioritizes workload to effectively accomplish goals. \u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ol\u0026gt;\n\u0026lt;li\u0026gt;Communicates clearly and effectively with clinicians, nursing and research staff, and research subjects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Check-in and report with the Lead Research Coordinator and/or RN at the start and end of each shift and provide a complete outgoing report.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sign / initial / and date all documents that were worked on during shift prior to leaving.\u0026lt;/li\u0026gt;\n\u0026lt;/ol\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;SCHEDULE\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Shift availability varies depending upon the type and number of active research protocols being executed. Shift may range from 4 to 12 hours. Some flexibility may be possible depending upon the protocol.\u0026amp;nbsp;RNs are strongly encouraged to attend monthly meetings led by the Lead Research Nurse. These meetings may include protocol and skills training, updates, and other topics as needed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$55\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$60 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005108009,"name":"Clinical: Nurses \u0026 Infusionists","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4121261009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4082294009,"location":{"name":"Atlanta, Georgia"},"metadata":null,"id":4121261009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"144","title":"PRN Psychometric Rater","company_name":"Headlands Research","first_published":"2026-02-11T17:12:14-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Clinical Research Atlanta, a Headlands Research site located in Stockbridge, GA, is seeking someone with experience providing clinical neurologic assessments to assess the adult patients participating in our clinical research trials. The Clinical Rater is responsible for administering and evaluating study-specific quantitative and qualitative scales and psychometric tests as part of a clinical team investigating pharmaceutical treatments for those with memory disorders.\u0026amp;nbsp; The Clinical Rater follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform required testing and related research activities.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; PRN\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel Required:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; 0%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Stockbridge, GA (no capability for remote work)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp; \u0026lt;/strong\u0026gt;As needed,\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;Monday - Friday, regular business hours\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administer study-specific clinical scales and psychometric tests, specifically CDR (Clinical Dementia Rating), PACC-5 (Preclinical Alzheimer\u0026#39;s Cognitive Composite 5)+, and evaluate results to determine study eligibility under the supervision of the lead physician.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct in-person cognitive, diagnostic, and clinical assessments of study participants, as well as caregiver interviews, for clinical trials in accordance to study protocol guidelines, FDA, and GCP.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;This position is responsible for ensuring that the data collection is in congruence with the philosophy and mission of the company, as well as with the specific scale administration guidelines, study protocol guidelines, GCP, and federal and local laws.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Actively work to maintain consistency in the performance of ratings over time for individual subjects to ensure efficacy and prevent rater drift\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Articulate ratings issues to lead physician, study sponsors or CROs, and other necessary individuals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate, complete, and timely visit source documentation including any sponsor-required information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond promptly to questions and feedback regarding rating assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure subject/patient safety by appropriately assessing and responding to any potential for harm to self or others and reporting it appropriately per company policy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate flow of professional and timely communication with subjects/patients, staff, referral sources, study sponsors or CROs, study monitors, auditors, and any central ratings group hired by the study sponsor.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete all study queries in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide appropriate community resource referrals to subjects, caretakers, and family, as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Master\u0026#39;s Degree or higher in Nursing or Psychology (or related field) required\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Will accept those with RN licenses with 2+ years of work experience administering and evaluating patients using CDR assessments in leau of Master\u0026#39;s degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Will accept those with Bachelor\u0026#39;s Degree in Psychology or related field and 2+ years of experience administering and evaluating patients using CDR assessments in leau of Master\u0026#39;s degree\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience administering Clinical Dementia Rating (CDR) scales to adults required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous experience serving as a Psychometrist, Psychometrician, or Clinical Rater on a clinical research trial highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, both verbal and written\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of integrity; trustworthy \u0026amp;amp; reliable\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in positions requiring a high amount of attention to details\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005107009,"name":"Clinical: Psychometric \u0026 Clinical Raters","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004748009,"name":"Georgia - Atlanta","location":"Stockbridge, Georgia, United States","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4194353009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4114421009,"location":{"name":"San Juan, Puerto Rico"},"metadata":null,"id":4194353009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"199","title":"Registered Nurse (RN) - Clinical Research","company_name":"Headlands Research","first_published":"2026-03-31T10:12:01-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About Us:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;CMRC Headlands is a premier clinical research site in San Juan, Puerto Rico. We conduct cutting-edge clinical trials in collaboration with global pharmaceutical sponsors, bringing medical innovation to our local communities. Our mission is to advance science while centering the patient experience at every stage of research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Summary:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;CMRC is seeking a\u0026amp;nbsp;\u0026lt;strong\u0026gt;seasoned, full-time Registered Nurse (RN)\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with strong clinical acumen and hands-on experience in both adult and pediatric settings. The ideal candidate has a background in hospital or private clinical practice, is passionate about patient-centered care, and thrives in a fast-paced, ambiguous, research-driven environment. This role requires a\u0026amp;nbsp;\u0026lt;strong\u0026gt;proactive self-starter\u0026lt;/strong\u0026gt;\u0026amp;nbsp;who can navigate complex protocols with clinical judgment, independence, and attention to detail. Bilingual fluency in\u0026amp;nbsp;\u0026lt;strong\u0026gt;English and Spanish\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;is essential.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and document pediatric and adult phlebotomy procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administer and document vital signs and clinical assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support all phases of patient interaction including screening, enrollment, dosing, and follow-ups\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as clinical support during study visits—monitor, document, and report on patient status and adverse events\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage specimen handling, labeling, storage, and timely shipment according to protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clinical oversight for study-related procedures to ensure safety and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and schedule research visits and procedures with precision and patient sensitivity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and interpret study protocols through a clinical lens to anticipate patient care needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate effectively with investigators, monitors, sponsors, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support study recruitment and patient outreach strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and organize source documentation and regulatory binders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare for monitoring visits and assist during sponsor or regulatory audits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as needed to support study execution\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Active and unrestricted \u0026lt;strong\u0026gt;Registered Nurse license\u0026lt;/strong\u0026gt;\u0026amp;nbsp;in Puerto Rico\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;6 years of experience\u0026lt;/strong\u0026gt;\u0026amp;nbsp;in a clinical setting (hospital or private practice)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of \u0026lt;strong\u0026gt;4 years drawing blood from both pediatric and adult patients\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid understanding of Good Clinical Practice (GCP) and/or willingness to undergo training\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfort working within protocol-driven environments with shifting timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to operate autonomously and take initiative within a small, agile team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient with electronic medical records, clinical data entry, and laboratory documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional organizational and multitasking skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills and compassionate bedside manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Fluent in English and Spanish \u0026lt;/strong\u0026gt;(written and verbal)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in clinical research or investigational trials is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with FDA, ICH-GCP, and HIPAA compliance standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience preparing for and interacting with clinical trial monitors\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005108009,"name":"Clinical: Nurses \u0026 Infusionists","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4007276009,"name":"Puerto Rico - San Juan","location":"San Juan, Puerto Rico","child_ids":[],"parent_id":4004733009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4246773009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4144126009,"location":{"name":"Chesterfield, Missouri"},"metadata":null,"id":4246773009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"253","title":"Research Assistant / Patient Recruitment","company_name":"Headlands Research","first_published":"2026-05-14T16:10:57-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Assistant / Patient Recruitment Assistant\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Chesterfield, MO\u0026amp;nbsp; 🏥 Site Name: Clinical Research Professionals | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Assistant (RA) / Patient Recruitment Specialist\u0026amp;nbsp;\u0026lt;/strong\u0026gt;for our Clinical Research Professionals site located in Chesterfield, MO. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;💼 The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a Clinical Research Assistant, you’ll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution—from subject screening, data entry, to patient recruitment. Your work will directly contribute to the success of new treatments in development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 4:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Onsite in Chesterfield, MO (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Clinical Manager\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;🌟What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Opportunities for professional development and career growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1696\u0026quot; data-end=\u0026quot;1801\u0026quot;\u0026gt;Assist research coordinators in \u0026lt;strong data-start=\u0026quot;1728\u0026quot; data-end=\u0026quot;1764\u0026quot;\u0026gt;conducting clinical trial visits\u0026lt;/strong\u0026gt; in compliance with study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1696\u0026quot; data-end=\u0026quot;1801\u0026quot;\u0026gt;Make outbound phone calls to \u0026lt;strong\u0026gt;recruit patients for upcoming trials\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1913\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1838\u0026quot;\u0026gt;Collect and record vital signs\u0026lt;/strong\u0026gt;, make study-related phone calls, and document data in electronic systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1916\u0026quot; data-end=\u0026quot;1984\u0026quot;\u0026gt;Support subject \u0026lt;strong data-start=\u0026quot;1932\u0026quot; data-end=\u0026quot;1957\u0026quot;\u0026gt;screening, enrollment\u0026lt;/strong\u0026gt;, and follow-up processes\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1987\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Review and verify study documentation for \u0026lt;strong data-start=\u0026quot;2029\u0026quot; data-end=\u0026quot;2058\u0026quot;\u0026gt;accuracy and completeness\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2063\u0026quot; data-end=\u0026quot;2150\u0026quot;\u0026gt;Maintain close communication with coordinators, investigators, and study participants\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Requirements:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with medical terminology and basic laboratory procedures preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience providing direct hands-on patient care preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;You must be comfortable sometimes spending long hours on the phone speaking with potential clinical trial participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical research experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2404\u0026quot; data-end=\u0026quot;2478\u0026quot;\u0026gt;Comfortable using multiple electronic data entry systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2481\u0026quot; data-end=\u0026quot;2586\u0026quot;\u0026gt;Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2589\u0026quot; data-end=\u0026quot;2686\u0026quot;\u0026gt;Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2689\u0026quot; data-end=\u0026quot;2746\u0026quot;\u0026gt;Passion for improving patient outcomes through research\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004743009,"name":"Missouri - St. Louis","location":"Chesterfield, Missouri, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4214334009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4125643009,"location":{"name":"Brownsville, Texas"},"metadata":null,"id":4214334009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"218","title":"Research Assistant / Pharmacy Technician","company_name":"Headlands Research","first_published":"2026-04-14T09:20:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Clinical Research Assistant\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Brownsville, TX | 🏥 Site Name: Headlands Research Brownsville | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We’re seeking a \u0026lt;strong\u0026gt;Clinical Research Assistant (RA)\u0026lt;/strong\u0026gt; for our clinical research site located in Brownsville, TX. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;💼 The Role:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a Clinical Research Assistant, you’ll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution—from subject screening to data entry. Your work will directly contribute to the success of new treatments in development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Type:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Regular Full-time Employee\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Mondays through Fridays, 8:00am - 5:00pm\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Brownsville, TX (no capabilities for remote or hybrid work)\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Reports to:\u0026amp;nbsp;\u0026lt;/strong\u0026gt; Site Director\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026amp;nbsp; Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;strong\u0026gt;🌟What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive pay + annual performance incentives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) plan with company match\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off (PTO) and company holidays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Opportunities for professional development and career growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A mission-driven culture focused on advancing medicine and improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;1696\u0026quot; data-end=\u0026quot;1801\u0026quot;\u0026gt;Assist research coordinators in \u0026lt;strong data-start=\u0026quot;1728\u0026quot; data-end=\u0026quot;1764\u0026quot;\u0026gt;conducting clinical trial visits\u0026lt;/strong\u0026gt; in compliance with study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1913\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1804\u0026quot; data-end=\u0026quot;1838\u0026quot;\u0026gt;Collect and record vital signs\u0026lt;/strong\u0026gt;, make study-related phone calls, and document data in electronic systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1916\u0026quot; data-end=\u0026quot;1984\u0026quot;\u0026gt;Support subject \u0026lt;strong data-start=\u0026quot;1932\u0026quot; data-end=\u0026quot;1957\u0026quot;\u0026gt;screening, enrollment\u0026lt;/strong\u0026gt;, and follow-up processes\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;1987\u0026quot; data-end=\u0026quot;2060\u0026quot;\u0026gt;Review and verify study documentation for \u0026lt;strong data-start=\u0026quot;2029\u0026quot; data-end=\u0026quot;2058\u0026quot;\u0026gt;accuracy and completeness\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2063\u0026quot; data-end=\u0026quot;2150\u0026quot;\u0026gt;Maintain close communication with coordinators, investigators, and study participants\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with medical terminology and basic laboratory procedures preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Certified Pharmacy Technician preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience providing direct hands-on patient care preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical research experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2404\u0026quot; data-end=\u0026quot;2478\u0026quot;\u0026gt;Comfortable using multiple electronic data entry systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2481\u0026quot; data-end=\u0026quot;2586\u0026quot;\u0026gt;Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2589\u0026quot; data-end=\u0026quot;2686\u0026quot;\u0026gt;Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2689\u0026quot; data-end=\u0026quot;2746\u0026quot;\u0026gt;Passion for improving patient outcomes through research\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005109009,"name":"Clinical: Research Assistants","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4205780009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4120235009,"location":{"name":"Riverside, California"},"metadata":null,"id":4205780009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"213","title":"Senior Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-04-01T14:13:46-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Want to be a part of a growing company that’s making a difference in our world? Look no further than Artemis Institute for Clinical Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A range of PPO and HMO medical plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;PPO and HMO dental plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Vision coverage, long term disability plan, and life/AD\u0026amp;amp;D coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401k plan\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid holidays and paid time off\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A welcoming work environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;The Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced Clinical Research Coordinator/Clinical Research Coordinator III for our Artemis Institute of Research clinical trial site located in Riverside, California. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Senior Clinical Research Coordinator manages study conduct from planning through study closeout.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position Type:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Full Time\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Pay Range:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;$76,000-$90,000/yr\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; \u0026amp;nbsp;Riverside, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Work Schedule:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;Monday through Friday, 9:30am-6:00pm\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending investigator meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing multiple studies as the primary coordinator and someone ready to take the next step in managing people\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Nursing license, medical assistant certificate or registration preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of two years of experience as a designated Clinical Research Coordinator on clinical trials required; sponsor-initiated and pharma clinical trials preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Previous clinical experience in a hands-on patient-facing role required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commitment and ability to deliver excellent customer service\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, punctual and responsible\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extremely well organized\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Trustworthy, reliable; attentive to details\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mature and pleasant demeanor\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to learn new tasks and grow with the company\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$76,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$90,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004736009,"name":"California - Riverside","location":"Riverside, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4266501009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4155801009,"location":{"name":"Escondido, California"},"metadata":null,"id":4266501009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"267","title":"Senior Clinical Research Coordinator","company_name":"Headlands Research","first_published":"2026-06-02T17:30:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;668\u0026quot; data-end=\u0026quot;792\u0026quot;\u0026gt;📍 Escondido, CA\u0026lt;br data-start=\u0026quot;687\u0026quot; data-end=\u0026quot;690\u0026quot;\u0026gt;🏥 AMCR Institute (a Headlands Research site)\u0026lt;br data-start=\u0026quot;748\u0026quot; data-end=\u0026quot;751\u0026quot;\u0026gt;🕒 Full-time \u0026lt;strong\u0026gt;|\u0026lt;/strong\u0026gt; Onsite (no opportunities for hybrid or remote)\u0026lt;/p\u0026gt;\n\u0026lt;h3 data-start=\u0026quot;794\u0026quot; data-end=\u0026quot;876\u0026quot;\u0026gt;For experienced CRCs looking for stability, collaboration, and meaningful work\u0026lt;/h3\u0026gt;\n\u0026lt;p data-start=\u0026quot;877\u0026quot; data-end=\u0026quot;1122\u0026quot;\u0026gt;If you’re an experienced Clinical Research Coordinator who values\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;943\u0026quot; data-end=\u0026quot;1054\u0026quot;\u0026gt;strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance\u0026lt;/strong\u0026gt;, AMCR Institute may be the right next step in your career.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;Our Escondido site is known for its \u0026lt;strong data-start=\u0026quot;1159\u0026quot; data-end=\u0026quot;1235\u0026quot;\u0026gt;depth of experience, thoughtful study execution, and team-based approach\u0026lt;/strong\u0026gt; to clinical research—particularly in metabolic studies.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1124\u0026quot; data-end=\u0026quot;1323\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;1325\u0026quot; data-end=\u0026quot;1328\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;1330\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;1333\u0026quot; data-end=\u0026quot;1366\u0026quot;\u0026gt;About AMCR Institute\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials. The site conducts studies focused on pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines. With a passionate and experienced team, AMCR Institute partners with sponsors and CROs to deliver meticulous research while prioritizing the care, safety, and confidentiality of every participant. By accelerating access to innovative therapies, the site makes a meaningful difference in the lives of the many affected by metabolic and immunologic conditions.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;1367\u0026quot; data-end=\u0026quot;1636\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;2096\u0026quot; data-end=\u0026quot;2099\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;2101\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2104\u0026quot; data-end=\u0026quot;2142\u0026quot;\u0026gt;Why Experienced CRCs Choose AMCR\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2145\u0026quot; data-end=\u0026quot;2212\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;2215\u0026quot; data-end=\u0026quot;2251\u0026quot;\u0026gt;Multi-disciplinary collaboration\u0026lt;/strong\u0026gt;\u0026amp;nbsp;with seasoned investigators and clinical staff\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2303\u0026quot; data-end=\u0026quot;2346\u0026quot;\u0026gt;Strong operational support and clear SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2349\u0026quot; data-end=\u0026quot;2420\u0026quot;\u0026gt;Exposure to complex, meaningful studies—not just high-volume turnover\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2487\u0026quot; data-end=\u0026quot;2555\u0026quot;\u0026gt;Backing of a growing research network with resources and stability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;This role is ideal for CRCs who enjoy\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2595\u0026quot; data-end=\u0026quot;2619\u0026quot;\u0026gt;owning their studies\u0026lt;/strong\u0026gt;, working with\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;2634\u0026quot; data-end=\u0026quot;2653\u0026quot;\u0026gt;competent teams\u0026lt;/strong\u0026gt;, and being trusted to execute with precision.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Provide the highest level of care for study patients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Deliver excellent customer service to pharmaceutical clients\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Coordinate all aspects of assigned clinical trials from site initiation through close-out\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Manage subject recruitment, informed consent, and retention activities\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Ensure timely EDC data entry and resolution of queries\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Report and follow up on AEs, SAEs, and protocol deviations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Collaborate with investigators, sponsors/CROs, labs, and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Prepare for and participate in monitoring visits, audits, and inspections\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain regulatory documentation and ensure training compliance for amendments and systems\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Attend investigator meetings and provide cross-functional support as needed\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Bachelor\u0026#39;s degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required.\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Experience with EDC, IVRS, and clinical research platforms\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Proficiency in medical terminology and clinical documentation\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Strong organizational skills with the ability to manage multiple studies\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Clear, professional verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;2557\u0026quot; data-end=\u0026quot;2699\u0026quot;\u0026gt;Comfortable working onsite in a collaborative, clinical environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;4906\u0026quot; data-end=\u0026quot;4909\u0026quot;\u0026gt;\n\u0026lt;h2 data-start=\u0026quot;4911\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;\u0026lt;strong data-start=\u0026quot;4914\u0026quot; data-end=\u0026quot;4942\u0026quot;\u0026gt;Who Thrives in This Role\u0026lt;/strong\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;CRCs who want\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;4959\u0026quot; data-end=\u0026quot;5001\u0026quot;\u0026gt;structure, support, and accountability\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those interested in taking the next step in managing people\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Professionals who value\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5030\u0026quot; data-end=\u0026quot;5053\u0026quot;\u0026gt;teamwork over silos\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Coordinators who care about data quality, patient experience, and compliance\u0026lt;/li\u0026gt;\n\u0026lt;li data-start=\u0026quot;4945\u0026quot; data-end=\u0026quot;5003\u0026quot;\u0026gt;Those ready to grow within a stable, well-established research site\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;hr data-start=\u0026quot;5210\u0026quot; data-end=\u0026quot;5213\u0026quot;\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;📬\u0026amp;nbsp;\u0026lt;strong data-start=\u0026quot;5218\u0026quot; data-end=\u0026quot;5233\u0026quot;\u0026gt;Apply today\u0026lt;/strong\u0026gt; if you’re looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p data-start=\u0026quot;5215\u0026quot; data-end=\u0026quot;5409\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-pay-transparency\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;pay-input\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;California Pay Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$80,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$90,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;177\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005106009,"name":"Clinical: Clinical Research Coordinators","child_ids":[],"parent_id":4005102009}],"offices":[{"id":4004738009,"name":"California - Escondido","location":"Escondido, California, United States","child_ids":[],"parent_id":4004735009}]},{"absolute_url":"https://job-boards.greenhouse.io/headlandsresearch/jobs/4202008009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_optional","internal_job_id":4117956009,"location":{"name":"Brownsville, Texas"},"metadata":null,"id":4202008009,"updated_at":"2026-06-05T17:10:24-04:00","requisition_id":"203","title":"Site Director - Clinical Research","company_name":"Headlands Research","first_published":"2026-03-30T11:29:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;📍 \u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; Brownsville, Texas | 🏥 Site Name: Headlands Research Brownsville | 🕒 Full-Time | 🧪 Clinical Research\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;span data-olk-copy-source=\u0026quot;MessageBody\u0026quot;\u0026gt;Are you a seasoned Clinical Research professional ready to lead at a higher level? Whether you’re a \u0026lt;strong\u0026gt;Senior/Lead CRC looking to step into site leadership\u0026lt;/strong\u0026gt;\u0026amp;nbsp;or a\u0026amp;nbsp;\u0026lt;strong\u0026gt;current Site Manager ready for broader ownership\u0026lt;/strong\u0026gt;, this is an opportunity to take full responsibility for site performance, team development, and clinical trial execution.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;As Site Director, you’ll move beyond day-to-day coordination to lead the\u0026amp;nbsp;\u0026lt;strong\u0026gt;strategy, operations, and growth\u0026lt;/strong\u0026gt;\u0026amp;nbsp;of a clinical research site—while still leveraging the deep operational expertise you built as a CRC.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the overall operational and financial performance of the clinical research site, including study execution, enrollment, and profitability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee all active clinical trials to ensure compliance with protocols, GCP, FDA regulations, and internal SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Monitor key performance metrics (e.g., enrollment, timelines, data quality) and implement improvements to drive site success\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Manage, coach, and develop a team of CRCs, research assistants, and site staff, fostering a high-performance and patient-focused culture\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Support hiring, onboarding, and ongoing performance management of site personnel\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Partner with internal teams to develop and execute patient recruitment strategies; monitor and optimize enrollment performance\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Build and maintain strong relationships with sponsors and CROs, ensuring high-quality delivery and repeat business\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Manage site budgets, staffing models, and resource allocation to optimize efficiency and financial outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Ensure audit readiness at all times; lead responses to audits, inspections, and quality findings\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Oversee regulatory documentation, source quality, and data integrity across all studies\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Identify operational challenges and implement scalable solutions to improve site performance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul type=\u0026quot;disc\u0026quot;\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;5+ years of clinical research site experience\u0026lt;/strong\u0026gt;, with a strong foundation as a CRC\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Experience as a\u0026amp;nbsp;\u0026lt;strong\u0026gt;Site Manager, Lead CRC, or in a supervisory role\u0026lt;/strong\u0026gt;\u0026amp;nbsp;strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Demonstrated ability to manage studies end-to-end, including enrollment and execution\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Prior experience\u0026amp;nbsp;\u0026lt;strong\u0026gt;leading, mentoring, or developing team members\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Strong knowledge of\u0026amp;nbsp;\u0026lt;strong\u0026gt;GCP, FDA regulations, and clinical trial operations\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Experience working with sponsors and CROs\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Proven ability to manage competing priorities in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Strong business mindset with exposure to site metrics,\u0026amp;nbsp;budgets, or performance goals\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;Bachelor’s degree preferred (or equivalent experience)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why This Role?\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Expand your scope\u0026lt;/strong\u0026gt;\u0026amp;nbsp;– Move from managing studies to leading an entire site\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Lead with credibility\u0026lt;/strong\u0026gt;\u0026amp;nbsp;– Your CRC experience will directly shape how you coach and develop your team\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Drive real impact\u0026lt;/strong\u0026gt;\u0026amp;nbsp;– Influence patient access to clinical trials and site-level success\u0026lt;/li\u0026gt;\n\u0026lt;li class=\u0026quot;x_MsoNormal\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Grow your career\u0026lt;/strong\u0026gt;\u0026amp;nbsp;– Clear path for advancement within a growing organization\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; 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data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;183\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;css-1hnm6b6\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-6qub7p\u0026quot; data-automation-id=\u0026quot;textSection\u0026quot;\u0026gt;\n\u0026lt;h3 id=\u0026quot;178\u0026quot; class=\u0026quot;css-1uppmgb\u0026quot;\u0026gt;Need Assistance?\u0026lt;/h3\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;div class=\u0026quot;css-vr2o4s\u0026quot;\u0026gt;\n\u0026lt;div id=\u0026quot;180\u0026quot; class=\u0026quot;css-cx1qpg\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;css-1b2vjjj\u0026quot; data-automation-id=\u0026quot;richText\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact\u0026amp;nbsp;\u0026lt;span class=\u0026quot;WOG1\u0026quot;\u0026gt;recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\u0026lt;/span\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005116009,"name":"Operations \u0026 Site Leadership","child_ids":[],"parent_id":4005103009}],"offices":[{"id":4004742009,"name":"Texas - Brownsville","location":"Brownsville, Texas, United States","child_ids":[],"parent_id":4004734009}]}],"meta":{"total":69}}