{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4670967006","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":4542459006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4670967006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"347","title":"Accounts Receivable (AR)  Manager","company_name":"Iterative Health","first_published":"2026-04-08T09:54:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly organized and experienced Accounts Receivable (AR) Manager to lead our AR operations with a focus on clinical research projects. The ideal candidate will have 5+ years of AR experience, including NetSuite proficiency, a strong background in collections management, and expertise in long-term, milestone-based contracts with partial payment structures. Experience in Real Time software and advanced Excel capabilities are also essential.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Location: Cambridge, MA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h4\u0026gt;\u0026lt;strong\u0026gt;Accounts Receivable \u0026amp;amp; Collections Management:\u0026lt;/strong\u0026gt;\u0026lt;/h4\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Run monthly AR reports, consolidate and prepare global aging by customer, location and business.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain executive AR dashboards including aging, DSO and other AR KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the AR reconciliation process between the GL and Real Time\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with project management and contract teams to align invoicing and collections with project milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and propose AR reserves.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare collections forecast reports.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Leverage NetSuite to manage AR operations and generate financial reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Use Real Time software to help track project data and integrate AR activities where appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely and accurate application of customer payments against open invoice within NetSuite.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee all AR functions including billing, invoicing, cash applications, and collections from an accounting perspective, partnering with the RCM team to ensure clinical research related receivables are properly recorded and reconciled.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage collections for\u0026lt;strong\u0026gt; \u0026lt;/strong\u0026gt;long-term contracts that include milestone-based and partial payments.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h4\u0026gt;\u0026lt;strong\u0026gt;Team Leadership \u0026amp;amp; Process Optimization:\u0026lt;/strong\u0026gt;\u0026lt;/h4\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supervise, mentor, and develop the AR function, coordinating with the RCM team as needed to improve performance and efficiency.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish KPIs for the AR function and drive process improvements to reduce aging and bad debt exposure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with other departments including Finance, Project Management, and Legal to resolve billing issues and support customer relationships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead AR-related audits and prepare supporting documentation as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h4\u0026gt;\u0026lt;strong\u0026gt;Industry-Specific Focus:\u0026lt;/strong\u0026gt;\u0026lt;/h4\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Apply knowledge of clinical research billing practices and revenue cycle requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure AR practices align with clinical study timelines, contracts, and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with other team members to ensure accurate financial reporting and support cost analysis initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelor’s degree in Accounting, Finance, or Business Administration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience: 5+ years of progressive AR/accounting experience, with at least 2 years in a managerial or supervisory role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 2 years of experience working within the healthcare industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record managing collections on milestone-based contracts with partial payment structures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in clinical research industry AR is required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in NetSuite and Real Time software.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of Microsoft Excel (pivot tables, VLOOKUP, etc.).\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;Exceptional attention to detail and organizational skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently and collaboratively in a fast-paced environment.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$95,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$135,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003490006,"name":"Finance \u0026 Accounting","child_ids":[],"parent_id":4003489006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4682181006","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":4548096006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4682181006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"390","title":"Business Development Associate - Cardiology","company_name":"Iterative Health","first_published":"2026-05-21T10:33:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About Iterative Health\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At\u0026lt;a href=\u0026quot;https://iterative.health/?utm_source=chatgpt.com\u0026quot;\u0026gt; Iterative Health\u0026lt;/a\u0026gt;, we are transforming clinical research through the power of AI, technology, and human expertise. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to improve patient outcomes. Through the Iterative Health Site Network — a premier network of 100+ clinical research sites across the US and Europe — we help expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why This Role Matters\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a Business Development Associate at Iterative Health, you will help build the front end of our growth strategy by identifying, researching, and engaging cardiovascular practices, physician groups, and strategic partnership opportunities across the United States.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role sits at the intersection of healthcare partnerships, business development, and corporate growth strategy reporting to the VP, Corporate Development. You will partner closely with senior leadership and Corporate Development to help source and develop qualified partnership and acquisition opportunities that support Iterative Health’s continued expansion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is not a traditional SDR role. While outbound outreach and pipeline generation are core components of the position, the role also provides exposure to healthcare partnerships, market strategy, and corporate development initiatives within a rapidly scaling healthcare organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for someone who is competitive, organized, intellectually curious, and excited to build a career in healthcare growth, partnerships, or corporate development.\u0026amp;nbsp;Strong performers will have the opportunity to grow into broader roles across partnerships, therapeutic area expansion, and corporate development as the company scales.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Where You’ll Drive Impact\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Research and identify independent groups, physician practices, and strategic partnership opportunities across prioritized markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build outbound target lists and prospecting campaigns to support pipeline generation efforts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct outbound outreach through email, phone, LinkedIn Sales Navigator, conferences, and additional engagement channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate qualified partnership opportunities and coordinate introductory discussions with senior leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Gather and synthesize information on prospective partners, including organizational structure, leadership teams, research capabilities, and growth initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support market mapping, target research, and strategic pipeline development activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate CRM documentation and outreach tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor outreach activity, sourcing metrics, and opportunity progression\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Iterative Health professionally in interactions with physicians, healthcare executives, and strategic partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute market insights and competitive intelligence to support growth strategy discussions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform 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;What You Bring to the Team\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;1–4 years of experience in outbound sales, business development, recruiting, lead generation, partnerships, or related experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills with confidence engaging external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail and follow-through\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competitive, self-motivated, and comfortable operating in a fast-paced growth environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intellectually curious with interest in healthcare strategy, partnerships, or corporate development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities and opportunities simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional presence and ability to communicate effectively with physicians and healthcare executives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using LinkedIn Sales Navigator, CRM platforms, or outbound prospecting tools preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Healthcare, healthcare services, or clinical research exposure is a plus, but not required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;How Success Is Measured\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Success in this role will be measured through:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Consistent generation of qualified partnership opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development and maintenance of high-quality target pipelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outbound engagement activity and prospect conversion rates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accuracy and organization of CRM and pipeline tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic insights and market intelligence contributed to leadership discussions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration, responsiveness, and ability to execute in a fast-moving environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;How We Work\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborative and low-ego team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High ownership and accountability culture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fast-paced and highly iterative growth environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Open communication and continuous learning mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mission-driven organization focused on improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable navigating evolving business priorities and opportunities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits That Support You\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe great teams do their best work when they feel supported — professionally and personally.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mental health and wellness support through Spring Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with a company match of up to 3% (up to $3,000 annually)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Weekly in-office lunch benefit every Tuesday\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;100% company-paid short-term and long-term disability coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Annual wellness and professional development stipend to support your health and growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$75,000\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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4027134006,"name":"626000 - Corporate Development ","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4682192006","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":4548101006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4682192006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"391","title":"Business Development Associate - Gastroenterology","company_name":"Iterative Health","first_published":"2026-05-21T10:34:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About Iterative Health\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At\u0026lt;a href=\u0026quot;https://iterative.health/?utm_source=chatgpt.com\u0026quot;\u0026gt; Iterative Health\u0026lt;/a\u0026gt;, we are transforming clinical research through the power of AI, technology, and human expertise. Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to improve patient outcomes. Through the Iterative Health Site Network — a premier network of 100+ clinical research sites across the US and Europe — we help expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why This Role Matters\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a Business Development Associate - Gastroenterology at Iterative Health, you will help build the front end of our growth strategy by identifying, researching, and engaging gastroenterology practices, physician groups, and strategic partnership opportunities across the United States.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role sits at the intersection of healthcare partnerships, business development, and corporate growth strategy reporting to the VP, Corporate Development. You will partner closely with senior leadership and Corporate Development to help source and develop qualified partnership and acquisition opportunities that support Iterative Health’s continued expansion.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is not a traditional SDR role. While outbound outreach and pipeline generation are core components of the position, the role also provides exposure to healthcare partnerships, market strategy, and corporate development initiatives within a rapidly scaling healthcare organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is an excellent opportunity for someone who is competitive, organized, intellectually curious, and excited to build a career in healthcare growth, partnerships, or corporate development.\u0026amp;nbsp;Strong performers will have the opportunity to grow into broader roles across partnerships, therapeutic area expansion, and corporate development as the company scales.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Where You’ll Drive Impact\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Research and identify independent groups, physician practices, and strategic partnership opportunities across prioritized markets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build outbound target lists and prospecting campaigns to support pipeline generation efforts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct outbound outreach through email, phone, LinkedIn Sales Navigator, conferences, and additional engagement channels\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate qualified partnership opportunities and coordinate introductory discussions with senior leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Gather and synthesize information on prospective partners, including organizational structure, leadership teams, research capabilities, and growth initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support market mapping, target research, and strategic pipeline development activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate CRM documentation and outreach tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor outreach activity, sourcing metrics, and opportunity progression\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Iterative Health professionally in interactions with physicians, healthcare executives, and strategic partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute market insights and competitive intelligence to support growth strategy discussions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform 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;What You Bring to the Team\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;1–4 years of experience in outbound sales, business development, recruiting, lead generation, partnerships, or related experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills with confidence engaging external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail and follow-through\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Competitive, self-motivated, and comfortable operating in a fast-paced growth environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intellectually curious with interest in healthcare strategy, partnerships, or corporate development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities and opportunities simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional presence and ability to communicate effectively with physicians and healthcare executives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using LinkedIn Sales Navigator, CRM platforms, or outbound prospecting tools preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Healthcare, healthcare services, or clinical research exposure is a plus, but not required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;How Success Is Measured\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Success in this role will be measured through:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Consistent generation of qualified partnership opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development and maintenance of high-quality target pipelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Outbound engagement activity and prospect conversion rates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accuracy and organization of CRM and pipeline tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic insights and market intelligence contributed to leadership discussions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration, responsiveness, and ability to execute in a fast-moving environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;How We Work\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaborative and low-ego team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High ownership and accountability culture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fast-paced and highly iterative growth environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Open communication and continuous learning mindset\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mission-driven organization focused on improving patient outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable navigating evolving business priorities and opportunities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Benefits That Support You\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe great teams do their best work when they feel supported — professionally and personally.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mental health and wellness support through Spring Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;401(k) program with a company match of up to 3% (up to $3,000 annually)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Weekly in-office lunch benefit every Tuesday\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;100% company-paid short-term and long-term disability coverage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Annual wellness and professional development stipend to support your health and growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;And more!\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$75,000\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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4027134006,"name":"626000 - Corporate Development ","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4664751006","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":4539469006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4664751006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"331","title":"Business Development Operations Manager","company_name":"Iterative Health","first_published":"2026-03-18T18:19:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a detail-oriented and commercially driven Manager of Business Development Operations to own end-to-end BD execution across our IBD, broader GI, and hepatology portfolio. This is a highly cross-functional role that sits at the intersection of commercial strategy, site operations, and sponsor partnerships. Reporting to the Director of Business Development, you will serve as the primary internal point of contact for new contracts and play a critical role in ensuring seamless execution from lead to signed study. You will own the processes, metrics, and relationships that keep our BD pipeline moving — and ultimately help bring new therapies to patients faster.\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;Own the end-to-end, internal business development process from initial sponsor engagement through contract execution, serving as the single internal touchpoint for new contracts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the cross-functional scoping and pricing process for new study opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keep the business development pipeline organized and visible by maintaining up-to-date reporting on where each opportunity stands\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Director of Business Development in preparing for key sponsor interactions, including developing pitches and proposals, building conference materials, and ensuring the team shows up well-prepared for high-stakes meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously identify opportunities to streamline and improve the business development process to accelerate deal pull-through and reduce time to contract close\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;4–7+ years of experience in life sciences, clinical trials, business development, or enterprise partnerships\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing end-to-end commercial processes, from scoping and pricing through contract execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaborator with a track record of working effectively across clinical, operations, and legal teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with strong attention to detail and ability to manage multiple deals and workstreams simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and relationship management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working in a fast-paced, high-growth environment with competing priorities\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;Experience in gastroenterology, hepatology, or adjacent therapeutic areas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of the clinical trials landscape\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in healthcare or business (MBA, MPH, or equivalent)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York 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;$140,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003481006,"name":"Life Sciences","child_ids":[],"parent_id":4020753006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4656833006","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":4535374006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4656833006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"313","title":"Clinical Data Manager","company_name":"Iterative Health","first_published":"2026-02-25T09:11:47-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager, Pre-Screening owns the top of the patient funnel for Iterative Health studies, including leading indicators on screenings, randomizations, and funnel volume / health. They will manage a team who performs EHR chart review to identify potential candidates for trial enrollment and are responsible for ensuring that every trial Iterative Health supports receives the right pre-screening support.\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;Execute human-in-the-loop component of EHR chart review and patient identification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and standardize EHR chart review processes and define metrics to measure quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Read and understand assigned study protocols to develop pre-screening approach and train team against\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own strategy to increase impact of EHR chart review\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure team achieves high performance on key success metrics and make recommendations on how to scale team capacity\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;As needed, provide coverage for team and perform EHR chart review\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support team members by resolving immediate issues and providing first-level guidance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own requirement development with Product team related to technologies developed for pre-screening\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical research protocols and manuscripts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Electronic Health Records systems\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional attention to detail and follow-up skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle and interact with confidential data securely and compliantly.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in software such as internet browsers, Adobe, Microsoft Office Suite (Word, Excel, PowerPoint, Outlook, Teams), and Salesforce\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;Clinical Research sector experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with reading and understanding clinical research manuscripts and protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with reviewing electronic health record data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Past experience working with Product teams to develop user requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience within a healthcare start-up preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Life and disability insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Parental leave\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stock options\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work hours\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unlimited paid time off\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Our Commitment to Diversity\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;At Iterative Health, we’re building a team that reflects the diversity of the patients we serve. We are committed to fostering an inclusive and equitable workplace, including our hiring process. If you require accommodations during the application or interview process, please reach out to: CandidateAccommodations@iterative.health.\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$97,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$120,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003482006,"name":"205000 - Professional Services","child_ids":[4026078006,4003486006,4003484006],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4682199006","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":4548105006,"location":{"name":"Cambridge, Massachusetts"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4682199006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"392","title":"Clinical Data Specialist - Site Operations","company_name":"Iterative Health","first_published":"2026-05-18T10:03:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we are pioneering the application of powerful, proprietary artificial intelligence tools to the practice of gastroenterology, cardiology, and drug development. We’ve set out to drastically improve clinical decision-making while meaningfully improving patient lives through better diagnosis, disease management, and treatment, leading to better health outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The \u0026lt;strong\u0026gt;Clinical Data Specialist \u0026lt;/strong\u0026gt;\u0026amp;nbsp;is responsible for supporting our clinical trial service operations through performing EHR chart review to identify patients who are candidates for clinical trials.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What you’ll be doing:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support research sites within the Iterative Health network by reviewing the electronic health records\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building a database of potential study candidates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Read and understand each assigned protocol to understand the applicable protocols and criteria of studies to determine specific patient population needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain documentation to track findings from Patient Pre-Screening\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend project meetings as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform administrative duties in conformity with company policies and procedures\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Skills:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience and competency in common office tools such as internet browsers, Adobe Acrobat, Microsoft Office (Word, Excel, PowerPoint), Google Workspace (Email, Drive, Sheets, Docs) and messaging platforms (Slack)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to quickly learn new systems and platforms such as Electronic Health Record systems, Customer Relationship Management systems (Salesforce) and clinical trial management systems (ie CTMS)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thrives when working within a high-paced, fluid environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent time management, planning, and organizational skills are required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and thorough follow-up skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable of handling and interacting with data in a confidential and compliant manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of tact, integrity, and professionalism\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;Clinical Research sector experience preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with reading and understanding clinical research manuscripts and protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with reviewing electronic health record data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with GCP guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience within a healthcare start-up preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003482006,"name":"205000 - Professional Services","child_ids":[4026078006,4003486006,4003484006],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4684335006","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":4549177006,"location":{"name":"Webster, TX"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4684335006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"399","title":"Clinical Research Assistant - RN - Webster, TX","company_name":"Iterative Health","first_published":"2026-05-27T10:18:25-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;If assigned, place IVs, administer IV medication, and fluids according to protocol. Monitor patients’ IV medications and tubing. Give intramuscular and subcutaneous injections according to protocol. Monitor patients during infusion and discharge patients as policies indicate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Registered Nurse\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1-2 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to execute on research tasks with guidance from more experienced staff, PIs, and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014498006,"name":"Webster, Texas","location":"Webster, Texas, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679234006","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":4546530006,"location":{"name":"Flowood, MS "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679234006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"371","title":"Clinical Research Coordinator - Flowood, MS ","company_name":"Iterative Health","first_published":"2026-05-05T17:07:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1-2 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to execute on research tasks with guidance from more experienced staff, PIs, and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014499006,"name":"Flowood, MS","location":"Flowood, Mississippi, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679966006","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":4546905006,"location":{"name":"New Albany, IN"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679966006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"383","title":"Clinical Research Coordinator I","company_name":"Iterative Health","first_published":"2026-05-07T15:39:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator I\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1-2 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to execute on research tasks with guidance from more experienced staff, PIs, and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014772006,"name":"New Albany, IN","location":"New Albany, Indiana, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679681006","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":4546751006,"location":{"name":"Cordova, TN "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679681006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"378","title":"Clinical Research Coordinator I ","company_name":"Iterative Health","first_published":"2026-05-07T10:16:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator I\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1-2 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to execute on research tasks with guidance from more experienced staff, PIs, and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014773006,"name":"Cordova, TN","location":"Cordova, Tennessee, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679691006","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":4546758006,"location":{"name":"Southaven, MS "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679691006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"381","title":"Clinical Research Coordinator II ","company_name":"Iterative Health","first_published":"2026-05-07T10:17:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to status updates to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4018107006,"name":"Southaven, MS ","location":"Southaven, Mississippi, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4649305006","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":4531744006,"location":{"name":"Des Plaines, IL "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4649305006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"290","title":"Clinical Research Coordinator II ","company_name":"Iterative Health","first_published":"2026-01-29T16:10:01-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014486006,"name":"Des Plaines, IL","location":"Des Plaines, Illinois, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4673446006","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":4543716006,"location":{"name":"Tacoma, WA"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4673446006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"352","title":"Clinical Research Coordinator II ","company_name":"Iterative Health","first_published":"2026-04-16T15:59:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management. Able to manage an increased number of studies and/or more complex studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Possible new bullet?\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4017797006,"name":"Tacoma","location":"Tacoma, Washington, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679964006","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":4546899006,"location":{"name":"New Albany, IN"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679964006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"382","title":"Clinical Research Coordinator II ","company_name":"Iterative Health","first_published":"2026-05-07T15:39:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to status updates to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014772006,"name":"New Albany, IN","location":"New Albany, Indiana, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4678280006","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":4546087006,"location":{"name":"Mansfield, TX"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4678280006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"366","title":"Clinical Research Coordinator II - Nurse ","company_name":"Iterative Health","first_published":"2026-05-01T18:46:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II - Nurse\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;If assigned, place IVs, administer IV medication, and fluids according to protocol. Monitor patients’ IV medications and tubing. Give intramuscular and subcutaneous injections according to protocol. Monitor patients during infusion and discharge patients as policies indicate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other site staff with coaching on best practices for clinical trials processes, patient interactions, data integrity, sponsor communication, and project management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Principal Investigators and referring positions to build understanding and enthusiasm for research opportunities for patients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance related to enrollment, screen fails, and protocol adherence\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess problem situations to identify causes, gather and process relevant information,\u0026amp;nbsp; generate possible solutions; make recommendations to management to resolve the situations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Registered Nurse\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4015332006,"name":"Mansfield, Tx","location":"Mansfield, Texas, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4676415006","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":4545208006,"location":{"name":"Southlake, TX "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4676415006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"361","title":"Clinical Research Coordinator II - Nurse ","company_name":"Iterative Health","first_published":"2026-04-28T15:58:57-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator II - Nurse\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management. Able to manage an increased number of studies and/or more complex studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;If assigned, place IVs, administer IV medication, and fluids according to protocol. Monitor patients’ IV medications and tubing. Give intramuscular and subcutaneous injections according to protocol. Monitor patients during infusion and discharge patients as policies indicate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Registered Nurse\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid nursing background, concentration, or willingness to obtain advanced knowledge in GI specialty\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4016898006,"name":"Southlake, TX ","location":"Southlake, Texas, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4684344006","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":4549184006,"location":{"name":"Richmond, VA"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4684344006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"400","title":"Clinical Research Coordinator II - Richmond, VA","company_name":"Iterative Health","first_published":"2026-05-27T10:18:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to status updates to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;em\u0026gt;IBD experience is a must\u0026lt;/em\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to own issues and problem solve independently\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4016259006,"name":"Richmond, VA","location":"Richmond, Virginia, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4667881006","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":4541003006,"location":{"name":"Cordova, TN "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4667881006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"340","title":"Clinical Research Coordinator I - Nurse ","company_name":"Iterative Health","first_published":"2026-03-27T15:38:58-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Clinical Research Coordinator I - Nurse\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;If assigned, place IVs, administer IV medication, and fluids according to protocol. Monitor patients’ IV medications and tubing. Give intramuscular and subcutaneous injections according to protocol. Monitor patients during infusion and discharge patients as policies indicate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014773006,"name":"Cordova, TN","location":"Cordova, Tennessee, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4678304006","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":4546101006,"location":{"name":"Sun City, AZ "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4678304006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"368","title":"Clinical Research Coordinator I - Nurse ","company_name":"Iterative Health","first_published":"2026-05-01T18:45:59-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator - Nurse. The CRC-RN supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities/Duties/Functions/Tasks:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Communicate study requirements to all individuals involved in the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement recruitment strategies in accordance with GI Alliance RESEARCH and IRB requirements and approvals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pre-screen and Screen subjects for eligibility using protocol specific inclusion and exclusion criteria.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Entry of participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding sources.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains adequate inventory of study supplies. When handling investigational drugs/devices, follows the sponsor protocol and/or GI Alliance RESEARCH Policy on Investigational Drug/Device Accountability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete study documentation and maintenance of study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains effective and ongoing communication with sponsor, research participants, site manager, Regional Director, and PI during the course of the study.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the day to day activities of the study including problem solving, communication and protocol management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collects and reports ongoing patient recruitment/ enrollment metrics to site manager and PI.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with GI Alliance RESEARCH compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance to the appropriate compliance office.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications and experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;RN license required\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;1-3 years of Clinical Research Coordinating experience preferred\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014497006,"name":"Sun City, AZ","location":"Sun City, Arizona, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4684357006","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":4549191006,"location":{"name":"Port Arthur, TX"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4684357006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"401","title":"Clinical Research Coordinator I - Port Arthur, TX","company_name":"Iterative Health","first_published":"2026-05-28T11:04:50-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 1-2 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to execute on research tasks with guidance from more experienced staff, PIs, and management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4018355006,"name":"Port Arthur, TX ","location":"Port Arthur, Texas, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4664486006","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":4539327006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4664486006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"330","title":"Clinical Research Finance Specialist ","company_name":"Iterative Health","first_published":"2026-03-18T09:01:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a motivated and detail-oriented Clinical Research Finance Specialist to join our growing Finance team. This role partners closely with the Finance Manager to support end-to-end accounts receivable operations across sponsor-funded clinical studies and internal research sites.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You will own core transactional AR workflows, including monitoring sponsor and site-level accounts, supporting timely collections, posting cash in RealTime CTMS, and assisting with invoicing as needed. This role requires close collaboration with internal teams, research sites, and sponsors and CROs to ensure accurate billing, timely cash application, and prompt resolution of outstanding balances.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate thrives in a fast-paced clinical research environment and enjoys balancing hands-on execution with cross-functional collaboration and continuous process improvement.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support day-to-day accounts receivable operations, including monitoring sponsor and site-level balances and assisting with timely collections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reconcile study-level balances and payment activity, identifying discrepancies and partnering with stakeholders to resolve issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately post cash receipts and payment details in RealTime CTMS and related financial systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and issue invoices for study activities and services in coordination with sponsor communications and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate professionally with sponsors and CROs regarding billing questions, payment status, and outstanding balances\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the preparation of AR aging schedules, financial summaries, and internal reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audits and financial reviews related to accounts receivable and billing activity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Clinical Operations, Site Finance, and Accounting to clarify billing terms and deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to ongoing process improvements to enhance AR efficiency, accuracy, and visibility\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide general finance support as needed to ensure smooth AR operations\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;Bachelor’s degree in Finance, Accounting, Business, or a related field (or equivalent practical experience)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years of experience in accounts receivable, billing, or finance operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong proficiency in Microsoft Excel, including data analysis and reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High attention to detail with the ability to manage multiple priorities and deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills, with a professional approach to external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with RealTime CTMS or similar clinical trial management and billing systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in healthcare, clinical research, or multi-site organizations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with sponsor contracts, clinical trial invoicing, or study-level financial reconciliation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$75,000\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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003490006,"name":"Finance \u0026 Accounting","child_ids":[],"parent_id":4003489006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4676147006","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":4545085006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4676147006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"359","title":"Clinical Research Systems Specialist","company_name":"Iterative Health","first_published":"2026-04-24T10:24:20-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is pioneering the use of artificial intelligence-based precision medicine in cardiology, with the aim of helping to optimize clinical trials. Ultimately, the company aims to establish more meaningful endpoints to serve as better predictors of both therapeutic response and disease outcomes. This is an exciting time in the Clinical Research industry! Our team is driving the advancement of research by implementing streamlined processes, with a mission of getting treatment options to patients in a faster, more efficient way.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;The Clinical Research Systems Specialist is responsible for supporting our clinical trial service operations through the development, maintenance, and quality assurance of administrative clinical trial materials.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;What you’ll be doing:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform and maintain study builds within CTMS system(s)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical research sites within their CTMS\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Clinical Research Specialists \u0026amp;amp; clinical research sites in EHR prescreening and management of Patient Findings Report\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct quality review and user acceptance testing of study builds to ensure alignment with protocol, sponsor requirements, and internal standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain databases/spreadsheets as necessary to facilitate tracking/documentation of departmental activities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide QC support for budget and contract team\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attend project meetings as needed\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Read and understand each assigned protocol\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regular reports to advise leadership of quality issues and to guide process corrections \u0026amp;amp; improvements\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform administrative duties in conformity with company policies and procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner cross-functionally with clinical operations, regulatory, finance, and site teams to support study launch and execution.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Skills:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Clinical Research Coordinator experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with CRIO, RealTime CTMS or similar clinical research technology platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Attention to detail and thorough follow-up skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capable of handling and interacting with data in a confidential and compliant manner\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to competently use and learn software such as internet browsers, Adobe, Microsoft Office (Word, Excel, PowerPoint, Outlook, Teams) and clinical trial management system (CTMS)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Intellectually curious\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hardworking, forward-thinking, credible, conscientious, and creative\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thrives when working within a high-paced, fluid environment\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent time management, planning, and organizational skills are required\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of tact, integrity, and professionalism\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience within a healthcare start-up preferable\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience reading and understanding clinical research manuscripts and protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with vendor management\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with ICH GCP/GDP guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with the following study documents: Budgets, CTAs, eCRF guidelines, lab manuals, pharmacy manuals, informed consent forms, annotated CRFs, etc.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York 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;$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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025810006,"name":"210020 - Growth","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4683962006","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":4548984006,"location":{"name":"NYC HQ"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4683962006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"397","title":"Director, Analytics","company_name":"Iterative Health","first_published":"2026-05-26T09:07:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is looking for a Director of Analytics to own how we define, measure, and improve performance across the business. This is a build role, you\u0026#39;ll be establishing the metrics layer, forecasting infrastructure, and reporting systems that our operational and commercial leaders depend on to make good decisions. You’ll be helping our leaders define what good looks like and help them unlock growth.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You\u0026#39;ll partner closely with teams across site operations, activations, capacity planning, and commercial to turn complex data into clear, actionable insights. The work spans everything from KPI definition and dashboard development to forecasting and trial enrollment modeling, with a direct line to the decisions that drive growth.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hands-on role. You\u0026#39;ll write SQL, build dashboards, and work directly in the data alongside the people you support. Over time you\u0026#39;ll grow a small team, but the expectation is that you\u0026#39;re a practitioner first.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Be the analytical partner operations and commercial leaders rely on\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Your primary customers are our operational and commercial leaders. They\u0026#39;re smart, data-savvy, and move fast. Your job is to make sure they have what they need to make good decisions — and to push back when the data tells a different story than the narrative.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Conduct deep-dive analyses on enrollment funnels, activation timelines, site performance, and commercial pipeline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Turn ambiguous business questions into structured analyses with clear, actionable outputs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support leadership reviews and board materials with clean data storytelling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enable team members across the business to pull and interpret their own data\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain trial enrollment and capacity models, both theoretical and bottoms-up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own trial enrollment forecasting, integrating site-level data, sponsor information with portfolio-level targets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scenario analyses to evaluate trade-offs across trials, sites, and investment options\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support quarterly planning and headcount decisions with rigorous, clearly communicated data\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Raise the analytics bar across the organization\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You\u0026#39;ll be setting the standard for how Iterative Health uses data. That means building the infrastructure and also shaping the culture around it.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design and maintain dashboards in SQL and BI tools (Power BI, Looker, or equivalent)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mentor teammates and cross-functional partners on analytical best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion data governance, documentation, and quality across the analytics function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hire and develop a small analytics team as the function matures\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Build the metrics layer from the ground up\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health has ambitious targets across patient enrollment, site activation, capacity growth, and commercial growth. Right now, the infrastructure to measure progress against those targets consistently and reliably is still being built. You\u0026#39;ll own that build.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and standardize KPIs across site operations, activations, patient funnel performance, and commercial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish a single source of truth including trusted definitions, clean lineage, documented logic\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Finance (who owns the Enterprise Data Warehouse) and the BI team to ensure clean upstream data and sound architecture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Replace manual spreadsheets and one-off analyses with reliable, self-serve reporting\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We\u0026#39;re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years in analytics, business intelligence, or a closely related function in a fast-moving environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert-level SQL and comfort working directly with large, messy, real-world datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience with BI tools (Power BI, Looker, Tableau, or equivalent)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of not just building KPI frameworks, dashboards, and automated reporting from scratch, but having strong business acumen and impact\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building forecasting or capacity models, not just reporting on actuals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication you can explain a complex model to a non-technical operator and make it land\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High ownership mindset you run problems to ground and don\u0026#39;t wait to be asked and want to build the roadmap for a function\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Strongly preferred\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in healthtech, clinical research, or life sciences, familiarity with clinical trials operations, enrollment funnels, or site networks is a real advantage\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Salesforce or revenue/commercial analytics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Python or R for advanced modeling\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with modern data warehouses (Snowflake, BigQuery, Redshift)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience building or managing a small analytics team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$160,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$215,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4005244006,"name":"Business Operations","child_ids":[],"parent_id":4020754006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4671523006","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":4542742006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4671523006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"350","title":"Director, Compliance","company_name":"Iterative Health","first_published":"2026-04-09T13:33:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h2\u0026gt;Position Overview\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a detail-oriented Director, Compliance to join Iterative Health\u0026#39;s growing team in New York, NY or Cambridge, MA. This role will be instrumental in leading the strategic development of compliance programs to ensure our clinical trial optimization solutions meet all regulatory requirements across healthcare, clinical trials, and data privacy domains. The ideal candidate will have deep expertise in healthcare compliance frameworks and the ability to operationalize complex regulatory requirements in a fast-paced health tech environment.\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;Key Responsibilities\u0026lt;/h2\u0026gt;\n\u0026lt;h3\u0026gt;Regulatory Compliance \u0026amp;amp; Risk Management\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experienced with the compliance aspects of clinical trial \u0026amp;amp; clinical research\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain comprehensive compliance with GDPR, HIPAA, and other applicable data privacy regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead SOC 2 Type II audit preparation and ongoing compliance, including controls documentation and evidence collection\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement compliance policies and procedures specific to clinical trial technologies and healthcare AI solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to Anti-Kickback Statute, Stark Law, and PhRMA Code requirements in all business relationships\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor evolving AI regulations and their impact on clinical trial optimization platforms\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Quality Management \u0026amp;amp; Documentation\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee Quality Management System (QMS) in partnership with other team members, for maintenance and contractual compliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain comprehensive record retention policies across clinical, regulatory, and business functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage document control processes for clinical protocols, compliance documentation, and regulatory correspondence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with clinical operations team to ensure GCP compliance in trial management and data collection\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Contract \u0026amp;amp; Vendor Compliance\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Review and negotiate compliance terms in customer agreements, vendor contracts, and clinical trial agreements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct vendor risk assessments and ongoing compliance monitoring for third-party service providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure contract compliance with healthcare customer requirements, including BAAs and data processing agreements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support commercial team with compliance aspects of customer onboarding and due diligence processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Training \u0026amp;amp; Cross-Functional Support\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and deliver compliance training programs for employees across all functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as primary compliance liaison with external auditors, regulators, and certification bodies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with legal, clinical, and product teams on regulatory strategy and risk mitigation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain compliance calendar and ensure timely completion of regulatory filings and renewals\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;Required Qualifications\u0026lt;/h2\u0026gt;\n\u0026lt;h3\u0026gt;Education \u0026amp;amp; Experience\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Business, or a related field plus 8+ years of compliance experience in healthcare, biotech, or clinical research organizations; advanced degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;OR Juris Doctor (JD) or other advanced degree plus 5+ years of compliance experience in healthcare, biotech, or clinical research organizations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience with clinical trial regulations and GCP requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record managing compliance programs in regulated industries\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Technical Expertise\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Employment law and HR compliance expertise, including workplace privacy, salary transparency, employee data protection, and regulatory training requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Corporate governance and general business compliance including anti-corruption, export controls, and corporate record-keeping requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Privacy program management across all business functions, including vendor privacy assessments and cross-border data transfer compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Financial compliance awareness including regulatory reporting requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of GDPR and HIPAA requirements and implementation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with SOC 2 audits and information security compliance frameworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical research regulations (GCP, ICH guidelines, 21 CFR Part 11)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of AI/ML regulatory landscape in healthcare and clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Core Competencies\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills with ability to translate complex regulations into actionable policies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills for regulatory correspondence and training delivery\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project management experience with ability to manage multiple compliance initiatives simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented approach with strong documentation and process improvement capabilities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;Preferred Qualifications\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Professional certifications (CIPP, CISA, CCEP, CHRC, or similar compliance credentials)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with international regulations (EU Clinical Trials Regulation, other global markets)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in clinical research or pharmaceutical compliance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with AI ethics and algorithmic bias considerations in healthcare\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with healthcare technology or SaaS compliance programs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$160,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$190,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003492006,"name":"Legal","child_ids":[],"parent_id":4003489006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679532006","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":4546690006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679532006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"376","title":"Director, Site Performance \u0026 Solutions (Cardiology)","company_name":"Iterative Health","first_published":"2026-05-06T12:34:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Director, Site Performance \u0026amp;amp; Solutions (Cardiology), you will report to the VP, Growth and own the performance of Iterative Health’s central clinical services that are delivered to our cardiology research sites as performance-enabling solutions, including pre-screening, regulatory support, and eSource. Your two core mandates are: owning the operating model for the central research support services we deliver to sites, and ensuring the network consistently hits and improves its activation and randomization targets.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a role for someone who is deeply grounded in research operations, relentlessly data-driven, and capable of diagnosing performance improvement opportunities quickly and implementing solutions at a high standard. You will serve as a “product owner” for our suite of site solutions, continuously improving how they are designed and delivered. When performance gaps emerge, you will be the person who figures out what is wrong and drives the fix.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Network Performance Ownership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own activation and randomization performance across IH’s cardiology site network as the single accountable leader.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor site and network-level performance metrics continuously, identifying trends, risks, and gaps before they escalate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understand the key levers that drive enrollment performance and ensure they are being optimized, consistently and systematically, across the network.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;When performance falls short, diagnose root causes quickly, develop a clear plan of action, and drive execution until the issue is resolved.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Operating Model \u0026amp;amp; Solution Ownership\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the accountable owner for IH’s cardiology central research support services, including regulatory support, pre-screening and eSource.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own the design, execution, and continuous improvement of the operating model for each service, treating them as products with clear performance standards and measurable outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and track service-level KPIs for each function; use performance data to surface improvement opportunities and raise the quality bar.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop scalable workflows and best practices that can be deployed consistently across the network.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the connective tissue between site-level performance trends and central service teams, ensuring the right resources are allocated where they will have the greatest impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collect and synthesize site feedback to inform service improvements and partner with cross-functional teams to implement solutions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Team Leadership \u0026amp;amp; Management\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Directly manage and develop a multidisciplinary team of clinical research specialists, e-source specialists, pre-screeners, and regulatory specialists\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Set clear goals and performance expectations for each function, provide ongoing coaching and development, and foster a high-performance team culture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure each team is properly resourced, trained, and equipped to deliver their services at the standard required to drive strong site outcomes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA or higher degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of clinical research experience, with deep familiarity with research operations and trial execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated proficiency with clinical research systems and tools, including CTMS and pre-screening workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to use data to diagnose performance problems, identify improvement opportunities, and drive decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of building and improving operating models or service delivery processes in a clinical research context\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven people management experience, with a track record of leading, developing, and holding accountable clinical research teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities, meet deadlines, and operate effectively in a fast-paced, evolving environment\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 a director-level or senior management role within a site network, CRO, or health tech organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience owning enrollment or operational performance metrics at a network or program level\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cardiology-specific clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$170,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$215,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025810006,"name":"210020 - Growth","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679507006","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":4546678006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679507006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"374","title":"Director, Strategy \u0026 Operations - Growth","company_name":"Iterative Health","first_published":"2026-05-06T11:59:54-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Director, Strategy \u0026amp;amp; Operations - Growth, you will report to the VP, Growth and serve as the leader of Iterative Health\u0026#39;s biological specimen collections business. This is a senior, highly autonomous role for an operator who is equally comfortable setting strategy and rolling up their sleeves to execute. You will own the go-to-market strategy, lead the full build-out of the business, and hold accountability for performance. You will also lead and develop the team that runs the day-to-day of collections operations. The ideal candidate brings a strong strategic and analytical foundation from management consulting or a high-growth startup environment, paired with the operational horsepower and ownership mindset to build something from the ground up.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Go-to-Market Strategy\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own the go-to-market strategy for Iterative Health\u0026#39;s biological specimen collections business — defining the service offering, target customer segments, competitive positioning, and path to scale\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define what we sell and how we sell it: Work with Business Development to scope the collections service model, establish pricing frameworks, and develop the materials and narrative needed to bring the offering to market\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Identify and size the resourcing, infrastructure, and capability requirements needed to support the strategy and inform investment decisions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Business Build-Out\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Lead the end-to-end build-out of the biological specimen collections business — standing up operational capabilities, and establishing the processes and infrastructure needed to execute at scale\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own vendor contracting and relationships, including selection, negotiation, onboarding, and ongoing performance management for all collections-related vendors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with the Business Development team to develop and progress a pipeline of collections studies, supporting sponsor engagement and proposal development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work cross-functionally with site operations leaders to identify and onboard the right site network to support collections studies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Business Performance Ownership\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own execution quality and sponsor satisfaction on active collections studies, serving as the senior point of escalation and ensuring trials are delivered to the highest standard\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and track KPIs across the business; use performance data to identify gaps, course-correct quickly, and communicate progress to senior leadership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Team Leadership\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, develop, and hold accountable a team that includes pre-screeners, central Clinical Research Coordinators, and a Clinical Operations Manager — setting clear performance targets and maintaining a high-performance culture\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Train team members on workflows, protocols, and quality standards, and ensure the team has the tools, processes, and support needed to execute at pace\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Set the operational tempo for the team — running structured operations, maintaining visibility into study and team performance, and driving accountability at every level\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;BS/BA or higher degree; advanced degree (MBA, MPH, or equivalent) strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of experience in a strategic and operational role, with meaningful exposure to building or scaling a business — prior experience in management consulting, a high-growth startup, or a general management capacity is strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading cross-functional build-outs — standing up new capabilities, managing vendors, and driving commercial pipelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven people leadership experience with the ability to recruit, develop, and hold accountable a high-performing team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional organizational and project management skills with the ability to manage multiple high-stakes workstreams simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong executive presence and communication skills — able to represent the business credibly with sponsors, vendors, and senior internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating with significant autonomy and building structure in ambiguous, fast-moving environments\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;Experience in life sciences, clinical research, or healthcare services — particularly in biological specimen collections studies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$175,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$225,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025810006,"name":"210020 - Growth","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4671351006","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":4542663006,"location":{"name":"Cambridge, Massachusetts, United States, Dallas, Texas, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4671351006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"349","title":"eSource Manager","company_name":"Iterative Health","first_published":"2026-04-09T10:09:30-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Manager of the eSource team is accountable for owning and optimizing the development,\u0026amp;nbsp; quality and standardization of all CTMS study templates, including study shells, financial templates, and eSource templates. This role ensures that all templates are compliant with Clinical Research and Good Clinical Practice (GCP) requirements, and operationally usable across sites and studies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The manager drives the execution of scalable playbooks, monitors performance through defined KPIs, and supports alignment with Clinical Operation milestones. The role serves as the primary owner for quality, readiness, and usability of all CTMS templates, as well as continuous improvement, while collaborating cross-functionally to support efficient study startup and execution.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a hands-on leadership role requiring both team management and direct contribution to template development, quality assurance, and process improvement.\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 manage the eSource team to deliver high-quality, compliant, and operationally effective templates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee daily operations, workload prioritization, and resource planning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive accountability within the team through clear expectations and performance management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor performance metrics and KPIs related to template quality, turnaround time, and operational impact\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Sr Director of Site Solutions to align team strategy with departmental goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support and execute the strategic vision for eSource and study template standardization across all studies and sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and maintain comprehensive operational playbooks governing the creation, validation, and lifecycle management of CTMS templates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all templates (Study Shells, Financial Templates, eSource Templates) align with Clinical Research standards and GCP best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own end-to-end QA/QC processes for all templates, ensuring readiness, completeness, accuracy, and usability prior to deployment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and enforce template governance frameworks, including version control, validation protocols, and audit readiness\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and manage timelines for template development aligned with regulatory and operational milestones (e.g., feasibility, study startup, SIV readiness)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to streamline and standardize template development to reduce redundancy and improve efficiency across studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implement continuous improvement processes based on user feedback, audit findings, and operational performance metrics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the subject matter expert (SME) for CTMS template design and eSource best practices\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams to ensure templates meet downstream workflow needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support training of cross-functional users\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support hiring, onboarding, and development of eSource team members\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Life Sciences, Healthcare Administration, or a related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience in clinical research operations, CTMS management, or study startup\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of GCP, regulatory requirements, and clinical workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience developing and building SOPs, playbooks, or standardized operational frameworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with RealTime SOMS/CTMS platform\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience in QA/QC, audit readiness, and validation of clinical research documentation or systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills with the ability to manage timelines across multiple studies and stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to define and track KPIs and drive performance outcomes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent attention to detail with a focus on data accuracy, completeness, and usability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience leading or managing a team in clinical research operations or technical services\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience building or managing eSource systems or digital clinical workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical trial budgeting and financial templates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in multi-site research networks or site management organizations (SMOs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with various CTMS platforms (e.g., CRIO, Medidata, or similar)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of integration between CTMS, EHR (e.g., eCW), and other systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting regulatory inspections or sponsor audits\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York 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;$130,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003482006,"name":"205000 - Professional Services","child_ids":[4026078006,4003486006,4003484006],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4014628006,"name":"Dallas, Tx","location":"Dallas, Texas, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4645212006","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":4529676006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4645212006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"284","title":"Finance Analyst ","company_name":"Iterative Health","first_published":"2026-01-23T09:01:31-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated Finance Analyst to join our growing team. In this role, you’ll partner closely with the Finance, Accounting and operational teams, as well as cross-functional stakeholders, to support strategic decision-making and optimize financial operations across the business. This is a high-impact role where you’ll gain hands-on experience supporting the financial operations of a rapidly scaling healthcare technology company. You will also play a key role in evolving our financial systems and infrastructure, particularly as we expand our joint venture (JV) partnerships and build for scale.\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;Develop and maintain robust financial models to evaluate revenue performance, key business metrics, and strategic growth initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present monthly reports to key business stakeholders, offering clear insights and transparency into financial performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the automation and accuracy of reports as the company builds out an EDW and implements Adaptive Insights\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic analysis and actionable recommendations to support decision-making across the business\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enhance forecast accuracy through deep understanding of financial and operational drivers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strengthen financial infrastructure and reporting processes to support scalability, efficiency, and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster strong collaboration between finance and business partners; work closely with operational teams to define department-level KPIs and identify opportunities for performance improvement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to high-impact financial initiatives, including board materials, investor communications, and other core finance functions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;2–3 years of experience in investment banking, consulting, or in a corporate finance / FP\u0026amp;amp;A related role at a high-growth startup\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial modeling, analytical and problem-solving skills, with attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with accounting principles and financial reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated interest in corporate finance and business operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Excel and PowerPoint, with strong presentation skills and the ability to communicate financial insights clearly to both technical and non-technical audiences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written, verbal, and interpersonal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work independently and manage cross-functional projects\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High level of ownership and a desire to learn and grow\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 with accounting systems (e.g., NetSuite)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accounting experience or relevant certification (e.g., working towards CFA certification)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$95,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$120,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003490006,"name":"Finance \u0026 Accounting","child_ids":[],"parent_id":4003489006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4681441006","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":4547720006,"location":{"name":"New York, New York or Cambridge, Massachusetts "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4681441006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"386","title":"Manager, Account Management - Life Sciences","company_name":"Iterative Health","first_published":"2026-05-13T15:43:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is redefining how clinical trials are conducted in IBD, and we’re looking for a commercial leader to help scale that impact. As Manager, Account Management - Life Sciences, you will drive the next chapter of Iterative Health’s growth in the biopharma and biotech ecosystem, owning and expanding relationships with our most important sponsors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a high-visibility, client-facing role for a builder - someone who thrives on creating value in complex partnerships, influencing senior stakeholders, and driving outcomes that matter. You’ll be the connective tissue between sponsors and Iterative’s internal teams, ensuring we deliver on every commitment while shaping how we evolve our solutions to meet the future of clinical research.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is ideal for a relationship-driven commercial leader who thrives in high-growth environments and enjoys building deep, strategic partnerships in the life sciences space.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US, Europe, and Asia, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking an experienced and execution-oriented Manager, Account Management - Life Sciencesto own day-to-day sponsor and CRO partnerships across our active clinical trial portfolio. This is a high-visibility, cross-functional role at the operational center of our business — sitting at the intersection of sponsor relationships, site operations, business operations, and clinical research delivery.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Associate Director of Life Sciences, you will serve as the primary point of accountability for a wide roster of accounts, leading high-impact meetings with sponsors and other research partners, driving trial recruitment and activation performance against committed targets, and acting as the connective tissue between commercial commitments and the operational teams that deliver against them. You will also help build the analytics, reporting, and tooling that scales sponsor account management as the network grows.\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;Own end-to-end client relationships across multiple active trials, including weekly operational meetings, quarterly business reviews, and general strategic conversations with sponsor and partner stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the escalation point for cross-functional issues spanning operations, legal, finance, and clinical regulatory - translating client needs into internal action and internal capacity into sponsor commitments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and present sponsor-facing materials including weekly status updates, quarterly business reviews, recruitment briefers, and ad-hoc analyses for executive and partner stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to commercial strategy and forecasting by partnering with the team on pipeline opportunities, feasibility responses, and contract amendments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain analytics and reporting tooling - including custom dashboards and AI-driven workflows - to scale account coverage and speed up decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mentor junior team members; set the bar for cross-functional communication, sponsor responsiveness, and operational rigor across the Life Sciences function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the company at sponsor meetings, industry conferences, and partner operational meetings as a senior commercial face of the network\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;4+ years of experience in alliance management, sponsor or partner-side trial delivery, or adjacent commercial roles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ownership of multi-stakeholder sponsor or partner relationships, including executive-facing communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication; able to write tight briefs and run a focused weekly meeting with multiple external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized and self-directed; comfortable carrying multiple active sponsor relationships and concurrent workstreams without external project management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commercial mindset with a bias toward action\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong cross-functional collaboration skills, with a track record of moving work through legal, finance, operations, and clinical functions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable in processing / analyzing disparate forms of data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working in a fast-paced, high-growth environment with competing priorities\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;Direct experience in GI, Hepatology, Cardiology, or other therapeutic areas\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with mid-size and large biopharma sponsors and global research partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with the systems used in modern clinical operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building or driving adoption of internal tooling, automation, or AI-assisted workflows\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;People management experience or demonstrated ability to lead through influence\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$115,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003481006,"name":"Life Sciences","child_ids":[],"parent_id":4020753006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679528006","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":4546685006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679528006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"375","title":"Manager, Growth Operations","company_name":"Iterative Health","first_published":"2026-05-06T12:34:01-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Manager, Growth, you will play a critical operational role at the center of Iterative Health\u0026#39;s two core growth engines in Cardiology: expanding our sponsor portfolio and scaling our site network. This is a high-visibility, high-impact role for a sharp operator who thrives on process ownership, cross-functional coordination, and getting things done in a fast-moving environment. You will own the internal mechanics of business development — keeping the pipeline moving, deals progressing, and sponsors well-served — while simultaneously driving the operational build-out of new clinical research sites from contract execution through first study activation. The ideal candidate brings a strategic and operational mindset, is energized by variety, and is able to manage multiple workstreams with rigor and speed.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Sponsor Growth: Business Development \u0026amp;amp; Alliance Management Support\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own the end-to-end internal business development process from initial sponsor engagement through contract execution, serving as the single internal touchpoint for new contracts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Keep the business development pipeline organized and visible by maintaining up-to-date reporting on opportunity status, next steps, and deal progression\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the Director of Research Partnerships in preparing for key sponsor interactions — developing pitches and proposals, building conference materials, and ensuring the team shows up well-prepared for high-stakes meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support sponsor account meetings through internal data gathering, performance reporting, and post-meeting follow-through\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Continuously identify opportunities to streamline and improve the business development process to accelerate deal pull-through and reduce time to contract close\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Site Network Growth: De Novo Site Builds\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with the Director of Clinical Research to support the end-to-end process of standing up de novo clinical research sites\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the operational connective tissue during site stand-up, tracking progress, surfacing blockers, and ensuring all cross-functional inputs come together on schedule\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with the Director of Clinical Research to continuously evaluate and improve the site stand-up process — identifying inefficiencies, building out playbooks, and creating repeatable frameworks that scale as the network grows\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;BS/BA or higher degree\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4+ years of experience in a strategic and operational role, such as management consulting, business operations, or growth/strategy at a high-growth startup\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to own and manage complex, cross-functional processes end-to-end with strong attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Excellent organizational skills with experience managing multiple projects and workstreams simultaneously in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communicator with the ability to synthesize information, build materials, and engage effectively with internal and external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working with ambiguity and building structure where it doesn\u0026#39;t yet exist\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;Experience in life sciences, clinical research, or healthcare\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical trial operations, site networks, or sponsor/CRO relationships\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$110,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$140,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025810006,"name":"210020 - Growth","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4683965006","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":4548985006,"location":{"name":"Mumbai, India"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4683965006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"398","title":"National Manager, Sites - India","company_name":"Iterative Health","first_published":"2026-05-23T14:56:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors\u0026#39; scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location:\u0026lt;/strong\u0026gt; India, Mumbai preferred due to current network footprint\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Why This Role Matters\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Seeking a highly organized and results-driven National Trial Site Support Manager to shape the our India organization from the ground up, lead clinical trial coordination and execution at multiple in-network sites across the country. This is a strategic role within Iterative Health, an innovative company expanding into India as a site support organization and reporting directly into the Head of ex-US Markets.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a person to help build and manage a team of CRCs, establish trial coordination and execution across sites/trials and pro-actively identify how clinical trials in India can be accelerated and where processes with Sites, Sponsors, and CROs can be improved.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role includes coordinating with Investigators, Sites and Sponsor/CRO teams, driving patient recruitment, overseeing clinical trial execution, managing team of site coordinators and ensuring adherence to the highest quality \u0026amp;amp; compliance standards. You will proactively manage operations in India, resolve roadblocks, escalate issues to relevant stakeholders, and maintain the highest quality of deliverables throughout while closely liaising with international Iterative Health counterparts.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Where You’ll Drive Impact\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Launch the Iterative Health site support organization structure in India\u0026lt;strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the foundational Clinical Research Coordinator until the broader team is in place, while supporting end-to-end study startup, site activation, and day-to-day clinical research operations across network sites in India, with the opportunity to help build and scale the organization’s national footprint and operational infrastructure from the ground up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support hiring and onboarding of Clinical Research Coordinators (CRC) for each site in the network. Supervise and mentor CRCs across studies and site network\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee and manage all aspects of study execution from startup to close-out across the site network to ensure timely delivery, highest quality and adherence to protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct routine oversight visits (on-site/remote) across network sites to review study progress, CRC performance, review protocol compliance, ensure audit readiness, escalate issues promptly, and maintain the highest quality of deliverables throughout the clinical trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Pro-actively work with the team to help our sites and sponsors to accelerate trial activation and execution timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive subject recruitment and retention strategies, ensuring monthly enrollment goals are met across clinical sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary liaison between the organization and site investigators, coordinators, and staff to maintain strong relationships and ensure prompt information sharing. Drive PI engagement on Iterative Health trials by providing proactive, hands-on support to principal investigators — helping them navigate study requirements, resolve questions, and stay closely connected to trial progress.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support pre-feasibility assessment and provide actionable operational insights including availability of patient pool, investigator competence and therapy experience, site capability and infrastructure to select best sites for new studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide weekly/ad-hoc updates on activation status, patient journeys, roadblocks, etc. to global\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform 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;What You Bring to the Team\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt; Minimum 8 years of project management, site management experience in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required Knowledge \u0026amp;amp; Skills:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in site management and leading teams of site coordinators and operations staff.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong technical knowledge, robust understanding of clinical trial processes, GCP, and country and international regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication, leadership, organizational and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple studies/sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience of managing clinical trials in Gastroenterology, Cardiology will be a strong plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel across site network in India and help grow the footprint in India\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Education:\u0026lt;/strong\u0026gt; B.A.M.S, B.H.M.S, B.U.M.S, M.Sc / B.Sc / M.Pharm / B.Pharm / Nursing / Biotechnology / Microbiology / Life Sciences/\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Additional Qualification\u0026lt;/strong\u0026gt;: Clinical Research Certification/Diploma\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Certification:\u0026lt;/strong\u0026gt; Candidates with a PMP certification will be given high priority.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel requirements:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Site Network Location (to date, growing):\u0026lt;/strong\u0026gt; Mumbai, Varanasi, Vellore\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Inception:\u0026lt;/strong\u0026gt; Role will likely require \u0026lt;strong\u0026gt;more travel across sites in the beginning\u0026lt;/strong\u0026gt;, particularly to build relationships and help kick off activities before the CRC team structure is fully established.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Mid-term/ongoing (once team is established)\u0026lt;/strong\u0026gt;: Every 6-10 weeks per site/ad-hoc as needed\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4027415006,"name":"210120 - Ex US ","child_ids":[],"parent_id":null}],"offices":[{"id":4018316006,"name":"International","location":null,"child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4612850006","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":4517932006,"location":{"name":"Cambridge, MA"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4612850006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"253","title":"Payroll Specialist","company_name":"Iterative Health","first_published":"2025-10-24T10:58:07-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;We are seeking an energetic, highly organized and detail-oriented individual to fill a full-time, Payroll Specialist role. The ideal candidate is an enthusiastic self-starter who is motivated to set and \u0026amp;nbsp;achieve goals and take initiative within the workplace. They are organized, professional\u0026amp;nbsp; and demonstrate excellent attention to detail. The successful candidate will be critical in reducing manual processing risks, ensuring regulatory compliance, systems automatizations and day-to-day payroll operations. This position will give you the opportunity \u0026amp;nbsp;to grow your payroll and accounting knowledge and experience.\u0026amp;nbsp; This role plays a key part in ensuring the accuracy and efficiency of our financial operations and will support broader financial reporting and compliance initiatives.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Process and finalize \u0026lt;strong\u0026gt;payroll runs \u0026lt;/strong\u0026gt;(Semi-Monthly, Bi-Weekly, Weekly, and specialized off-cycle runs) for all employees using our primary payroll platforms, \u0026lt;strong\u0026gt;Rippling and ADP\u0026lt;/strong\u0026gt;.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Verify all timecards, wage computation, statutory deductions, benefits deductions, garnishments, and employee changes for accuracy and compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage end-to-end processing, including reconciling final payroll previews and submitting funding requests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary subject matter expert for payroll and HRIS systems including \u0026lt;strong\u0026gt;Rippling, ADP, and BambooHR\u0026lt;/strong\u0026gt;.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Prepare payroll-related General Ledger (GL) entries into the \u0026lt;strong\u0026gt;NetSuite\u0026lt;/strong\u0026gt; accounting system, ensuring accurate cost center allocations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reconcile payroll accounts on a monthly basis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and reconcile bank account transactions related to payroll disbursements.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely and accurate processing of all federal, state, and local tax remittances, including quarterly and year-end reporting (W-2s, 1099s, 941a reports).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage \u0026lt;strong\u0026gt;new state registrations for employees\u0026lt;/strong\u0026gt; and quarterly \u0026lt;strong\u0026gt;Workers\u0026#39; Compensation (WC) tax reporting\u0026lt;/strong\u0026gt;.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Administer \u0026lt;strong\u0026gt;401K contribution processing\u0026lt;/strong\u0026gt;.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the \u0026lt;strong\u0026gt;annual 401K audit\u0026lt;/strong\u0026gt;..\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to and resolve employee inquiries regarding pay, deductions, and tax forms, reducing the administrative burden on the Accounting Manager.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Education:\u0026lt;/strong\u0026gt; Associate’s degree in Accounting, Finance, or a related field; Bachelor’s degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Experience:\u0026lt;/strong\u0026gt; 2+ years of dedicated payroll processing experience, ideally managing high-frequency (monthly, bi-weekly, weekly) and multi-state payroll.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;System Proficiency:\u0026lt;/strong\u0026gt; Proven, hands-on expertise with major systems including \u0026lt;strong\u0026gt;ADP, Rippling, Fidelity 401K, NetSuite, and advanced Microsoft Excel skills.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;Skills:\u0026lt;/strong\u0026gt; Exceptional attention to detail, strong analytical and problem-solving skills, and ability to handle confidential information with discretion.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with ADP, Rippling, Bamboo, NetSuite.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional certification (e.g., Fundamental Payroll Certification (FPC) or Certified Payroll Professional (CPP)).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;WorkDay Experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$63,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$88,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003489006,"name":"G\u0026A ","child_ids":[4003492006,4003490006],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4001636006,"name":"US Remote","location":"Remote","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4678430006","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":4546161006,"location":{"name":"NYC or Boston "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4678430006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"369","title":"People Business Partner","company_name":"Iterative Health","first_published":"2026-05-03T17:26:06-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;We are seeking a strategic and data-driven People Business Partner role to partner closely with leaders across corporate functions and site-based operational teams in support of a high performing, highly distributed healthcare services organization. This role will act as a trusted advisor, aligning people strategies with business priorities to support growth, scalability, and performance across the organization.\u0026amp;nbsp;Operating in a high-growth, M\u0026amp;amp;amp;A driven environment, this role requires a strong balance\u0026amp;nbsp;of strategic thinking and hands-on execution. The People Business Partner will play a\u0026amp;nbsp;key role driving organizational effectiveness, enabling leadership and supporting\u0026amp;nbsp;change initiatives while fostering a high-performing, mission-driven culture.\u0026amp;nbsp;This individual must be comfortable pivoting between both a strategic and hands-on\u0026amp;nbsp;level of engagement, with a strong focus on change and performance management,\u0026lt;br\u0026gt;talent/leadership development, organizational design, employee relations and integration.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;Key Responsibilities\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;Strategic Business Partnership\u0026lt;br\u0026gt;● Serve as a trusted advisor, coach and thought partner to department, team and\u0026amp;nbsp;operational leaders, providing guidance on organizational strategy, workforce\u0026amp;nbsp;planning, employee relations issues and talent implications of business decisions\u0026lt;br\u0026gt;● Translate business priorities into actionable HR strategies that drive growth, scalability, and operational excellence to enable a high performing and engaged\u0026amp;nbsp;workforce.\u0026lt;br\u0026gt;● Develop a deep understanding of IH business units, financial drivers, and market industry dynamics to proactively shape people initiatives that help transform the\u0026amp;nbsp;business as we grow and scale our infrastructure.\u0026lt;br\u0026gt;● Serve as a strategic liaison and advisor between the business and People Team\u0026amp;nbsp;Center of Excellence’s (COE) to align HR service delivery with business priorities\u0026lt;br\u0026gt;● Identify opportunities to implement data-informed people strategies that\u0026amp;nbsp;strengthen organizational health, culture and maturity while directly impacting\u0026amp;nbsp;leadership effectiveness and team performance\u0026lt;br\u0026gt;● Lead workforce planning with business partners, anticipating skills and\u0026amp;nbsp;capabilities needed to scale the organization beyond current state – develop\u0026amp;nbsp;plans in conjunction with TA to identify talent profiles and succession bench\u0026amp;nbsp;ready for promotion to increased level of scope and responsibility\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Talent and Performance Management\u0026lt;br\u0026gt;● Drive talent and performance management processes that reinforce\u0026amp;nbsp;accountability, ownership and high standards of behaviors / values alignment to\u0026amp;nbsp;support our high-performance culture\u0026lt;br\u0026gt;● Partner with leaders on succession planning, leadership development,\u0026amp;nbsp;compensation strategies and retention initiatives across the enterprise\u0026lt;br\u0026gt;● Use data and insights to inform talent decisions and effectively balance business\u0026amp;nbsp;needs with employee advocacy\u0026lt;br\u0026gt;● Coach and develop leaders to engage, motivate and lead high performing teams,\u0026amp;nbsp;identifying least effective performance and partnering with team leaders to\u0026amp;nbsp;address performance issues early on.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;Change Management and Culture\u0026lt;br\u0026gt;● Lead change management efforts across our growing and evolving\u0026amp;nbsp;teams/structures to support effective communication, accountability and\u0026amp;nbsp;alignment to our strategic priorities\u0026lt;br\u0026gt;● Champion a culture of innovation, collaboration, and continuous improvement\u0026amp;nbsp;aligned with Iterative Health’s mission\u0026lt;br\u0026gt;● Support leaders in navigating ambiguity and leading through transformational change as an organization, providing insights and serving as a “thought partner” on operational and people challenges that dynamic growth brings.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Employee Relations and Coaching\u0026lt;br\u0026gt;● Provide expert coaching on employee relations, leadership effectiveness, and\u0026amp;nbsp;team dynamics to enable a highly engaged, productive workforce while\u0026amp;nbsp;maintaining consistency and alignment to IH policies and procedures.\u0026lt;br\u0026gt;● Support positive culture building initiatives and drive employee engagement\u0026amp;nbsp;initiatives with team leaders to build highly engaged, motivated team members.\u0026lt;br\u0026gt;● Ensure compliance with employment laws and company policies – identify\u0026amp;nbsp;opportunities to improve, create and implement policies and procedures that\u0026amp;nbsp;balance business needs with operational realities\u0026amp;nbsp;M\u0026amp;amp;A \u0026lt;br\u0026gt;\u0026lt;br\u0026gt;HR Integration\u0026lt;br\u0026gt;● Partner with internal stakeholders including People COE’s on due diligence,\u0026amp;nbsp;integration planning, and execution as part of pre and post-acquisition integration\u0026amp;nbsp;process\u0026lt;br\u0026gt;● Support organizational design, talent assessment, and cultural integration efforts\u0026amp;nbsp;to ensure seamless onboarding of acquired entities and team members to IH\u0026lt;br\u0026gt;● Anticipate, identify and mitigate people-related risks associated with rapid growth\u0026amp;nbsp;and change, including supporting HR initiatives focused on harmonization of\u0026amp;nbsp;system, processes and policies across the growing enterprise.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;HR Program Execution\u0026lt;br\u0026gt;● Partner with COE to deliver best-in-class HR transformational initiatives to\u0026amp;nbsp;support a growing and scaling workforce\u0026lt;br\u0026gt;● Own HR projects in support of strategic HR agenda focused on employee\u0026amp;nbsp;engagement, leadership development, performance management, and\u0026amp;nbsp;operationalizing best in class people initiatives and infrastructure that will attract,\u0026amp;nbsp;develop and retain talent.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;Qualifications\u0026lt;br\u0026gt;● 7–10+ years of progressive HR experience, including working in a fast-scaling,\u0026amp;nbsp;high-growth, complex and ambiguous start-up environment\u0026lt;br\u0026gt;● Experience in healthcare, clinical research, medtech, life sciences, or related\u0026amp;nbsp;industries strongly preferred\u0026lt;br\u0026gt;● Experience supporting a highly distributed, growing multi-site location network\u0026amp;nbsp;both domestically and globally is strongly preferred\u0026lt;br\u0026gt;● Demonstrated experience across a wide range of HR functional domains\u0026lt;br\u0026gt;● Strong business acumen with the ability to link HR strategy to financial and\u0026amp;nbsp;operational outcomes\u0026lt;br\u0026gt;● Proven ability to communicate and influence senior leaders as well as operate as\u0026amp;nbsp;a strategic partner, understanding the operational and strategic priorities of the\u0026amp;nbsp;business and how people strategies can make an impact\u0026lt;br\u0026gt;● Experience in organizational design, change management, and talent strategy\u0026lt;br\u0026gt;● Data-driven, analytical mindset with comfort leveraging data and analytics to\u0026amp;nbsp;inform decisions\u0026lt;br\u0026gt;● Excellent communication, coaching, and stakeholder management skills\u0026lt;br\u0026gt;● Comfort navigating through ambiguity and managing multiple competing priorities\u0026lt;br\u0026gt;● A builder and inventor mindset – orientation towards thinking outside the box to\u0026amp;nbsp;pilot and test programs and initiatives to iterate before applying a one-size fits all\u0026amp;nbsp;approach.\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$110,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$145,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4027133006,"name":"640000 - People Operations ","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4594096006","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":4508491006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4594096006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"225","title":"Regional Director, Sites","company_name":"Iterative Health","first_published":"2025-08-18T00:53:21-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Regional Director is responsible for owning and optimizing site-level performance across a portfolio of GI-focused clinical research sites. This role ensures operational excellence by aligning teams around key performance goals, elevating site capabilities, and maintaining consistency in trial execution. As a strategic operations leader, the Regional Director plays a central role in connecting site level performance with broader business objectives.\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;Manages staff across multiple sites, ensuring execution is aligned with protocol, regulatory requirements, and IH standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Owns overall performance of assigned sites, including enrollment, data quality, compliance, and team culture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures sites are set up for success (i.e. staffed appropriately and equipped with the appropriate equipment and training) and makes recommendations to allocate resources based on business needs.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Builds strong relationships and collaborates with PIs to align their engagement with study goals and operational strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Influences study portfolio, optimizing for profitability and value to patients.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies and manages issues, concerns and problems related to site performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leads and develops CRCs, and other site-based research staff through clear expectations, performance coaching, and team development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serves as a visible, hands-on people manager who builds high-performing, accountable teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identifies levers to drive site level KPIs through monitoring KPIs and performance trends, escalating to appropriate parties.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Implements corrective actions or process improvements as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serves as the primary operational liaison between site staff and central functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drives a culture of ownership, collaboration, and continuous improvement across all assigned sites.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Knowledgeable about the critical elements for success in clinical trials: Ability to review protocols, programs, and assess the success of a project.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to influence change management and model flexibility\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Problem-Solving Skills: Ability to identify problems, develop and implement solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic Planning: Ability to plan for short, medium and long term success and make recommendations for growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use data as a tool, identify trends, and draw conclusions.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Project Management: Demonstrated ability to successfully manage people/projects.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive problem-solving abilities and follow-through.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Practices professionalism and integrity in all actions.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communication Skills: Excellent written and verbal communication skills.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of CTMS, eDC and other core research systems.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to travel: Up to 30% travel to provide operational oversight, hold team meetings, and attend other professional meetings/conferences as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience in managing a large site network and demonstrated success in achieving targets and optimizing operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with gastroenterology and/or hepatology studies.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We Offer\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical, dental, and vision insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Life and disability insurance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Parental leave\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stock options\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work hours\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Unlimited paid time off\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003482006,"name":"205000 - Professional Services","child_ids":[4026078006,4003486006,4003484006],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null},{"id":4001636006,"name":"US Remote","location":"Remote","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4674677006","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":4544384006,"location":{"name":"Brunswick, OH "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4674677006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"355","title":"Research Assistant - Brunswick, OH ","company_name":"Iterative Health","first_published":"2026-04-21T08:48:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Research Assistant\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, on-site Research Assistant (RA). The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site management. The primary responsibility of the RA is to assist the Clinical Research\u0026amp;nbsp; Coordinators with conduct of research studies. The RA supports and facilitates the daily\u0026amp;nbsp; clinical trial activities and plays a supportive role in the conduct of the study.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team with communicating study requirements to all individuals involved in the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements and approvals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team with screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or site policies on Investigational Drug/Device Accountability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in completing study documentation and maintenance of study files in accordance with sponsor requirements and site policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Aids the Study Team in maintaining effective and ongoing communication with sponsor, research participants, site management and PI during the course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Works with the Study Team to manage the day to day activities of the study including problem solving, communication and protocol management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collects and reports ongoing patient recruitment/ enrollment progress and metrics to site management and PI\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;As directed, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enter all patient visit data in e-CRF and CTMS on a daily basis or as directed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;High school diploma or equivalent. Some college preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 2 years in a healthcare setting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4017877006,"name":"Brunswick ","location":"Brunswick, Ohio, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4681487006","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":4547743006,"location":{"name":"Des Plaines, IL "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"In Person","value_type":"single_select"}],"id":4681487006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"387","title":"Senior Clinical Research Coordinator","company_name":"Iterative Health","first_published":"2026-05-13T17:00:44-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Senior Clinical Research Coordinator (Sr. CRC) in Des Plaines, Illinois. The Sr. CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other site staff with coaching on best practices for clinical trials processes, patient interactions, and project management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Principal Investigators and referring positions to build understanding and enthusiasm for research opportunities for patients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess problem situations to identify causes, gather and process relevant information, generate possible solutions; make recommendations to management to resolve the situations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, associate or bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;$35-$45 per hour\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014486006,"name":"Des Plaines, IL","location":"Des Plaines, Illinois, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4677975006","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":4545940006,"location":{"name":"Flowood, MS "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4677975006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"365","title":"Senior Clinical Research Coordinator ","company_name":"Iterative Health","first_published":"2026-05-01T10:59:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h1\u0026gt;Senior Clinical Research Coordinator\u0026lt;/h1\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Senior Clinical Research Coordinator (Sr. CRC). The Sr. CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication\u0026amp;nbsp; and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system\u0026amp;nbsp; on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site\u0026amp;nbsp; Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other site staff with coaching on best practices for clinical trials processes, patient interactions, and project management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Principal Investigators and referring positions to build understanding and enthusiasm for research opportunities for patients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess problem situations to identify causes, gather and process relevant information,\u0026amp;nbsp; generate possible solutions; make recommendations to management to resolve the situations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;New bullet ?\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and\u0026amp;nbsp; coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, Associates or Bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skils\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift up to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4014499006,"name":"Flowood, MS","location":"Flowood, Mississippi, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4679115006","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":4546486006,"location":{"name":"Toms River, NJ "},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4679115006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"370","title":"Senior Clinical Research Coordinator- Toms River, NJ ","company_name":"Iterative Health","first_published":"2026-05-06T15:03:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 18pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Senior Clinical Research Coordinator\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a full-time, experienced Senior Clinical Research Coordinator (Sr. CRC). The Sr. CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Responsibilities:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule all patient research visits and procedures consistent with protocol requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct patient visits as outlined within each study protocol\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Dispense study medication, collect vital signs and perform ECGs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform blood draws, process and ship specimens per study protocol and IATA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as point of contact for study participants\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adhere to Research SOPs, Good Clinical Practices, and the study protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all safety data is reviewed by the PI in a timely manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain inventory of study equipment and supplies onsite at all times\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support other site staff with coaching on best practices for clinical trials processes, patient interactions, and project management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work closely with Principal Investigators and referring positions to build understanding and enthusiasm for research opportunities for patients\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess problem situations to identify causes, gather and process relevant information, generate possible solutions; make recommendations to management to resolve the situations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule and prepare for monitor visits\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Iterative Health Expectations\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employees are expected to:\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform quality work within deadlines with or without direct supervision\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interact professionally with other employees, customers and suppliers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work effectively as a team contributor on all assignments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Qualifications\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical Assistant, LPN, associate or bachelor’s degree in a clinical or scientific-related discipline preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of clinical research experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in phlebotomy preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to read, interpret, and apply clinic policies and research protocols\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to use standard office software\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to lift to 25 pounds\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003484006,"name":"Clinical Services","child_ids":[],"parent_id":4003482006}],"offices":[{"id":4016377006,"name":"Toms River, NJ","location":"Toms River, New Jersey, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4671629006","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":4542801006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4671629006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"351","title":"Senior Clinical Research Finance Specialist ","company_name":"Iterative Health","first_published":"2026-05-12T10:51:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a motivated and detail-oriented Senior Clinical Research Finance Specialist to join our growing Finance team. This role partners closely with the Finance Manager to support end-to-end accounts receivable operations across sponsor-funded clinical studies and internal research sites.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You will own core transactional AR workflows, including monitoring sponsor and site-level accounts, supporting timely collections, posting cash in RealTime CTMS, and assisting with invoicing as needed. This role requires close collaboration with internal teams, research sites, and sponsors and CROs to ensure accurate billing, timely cash application, and prompt resolution of outstanding balances.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate thrives in a fast-paced clinical research environment and enjoys balancing hands-on execution with cross-functional collaboration and continuous process improvement.\u0026lt;/p\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own day-to-day accounts receivable operations for sponsor-funded studies and internal sites, ensuring accurate tracking of balances and timely collections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and reconcile study-level balances and payment activity, proactively identifying discrepancies and driving resolution with internal and external stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Accurately post cash receipts and payment details in RealTime CTMS and related financial systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and issue invoices for study activities and services in coordination with sponsor communications and internal teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key point of contact for sponsors and CROs regarding billing inquiries, payment status, and outstanding balances\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Analyze AR aging and payment trends, escalating risks and recommending actions to improve collections and cash flow\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in preparing AR aging schedules, financial summaries, and operational reporting for finance leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support internal audits, financial reviews, and documentation related to accounts receivable and billing activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Clinical Operations, Site Finance, and Accounting teams to clarify billing terms, milestone triggers, and contract deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to improve AR workflows, reporting, and system utilization to increase efficiency and financial transparency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to finance process documentation and help implement best practices across the organization\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Required Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Finance, Accounting, Business, or a related field (or equivalent practical experience)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026lt;strong\u0026gt;3–5+ years of experience\u0026lt;/strong\u0026gt; in accounts receivable, billing operations, or finance within a complex or multi-entity environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong proficiency in Microsoft Excel, including data analysis, reconciliation, and financial reporting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple priorities while maintaining strong attention to detail and accuracy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills with the ability to work effectively with internal stakeholders and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to independently manage operational finance processes and resolve issues proactively\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h1\u0026gt;\u0026lt;strong\u0026gt;Preferred Qualifications\u0026lt;/strong\u0026gt;\u0026lt;/h1\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with \u0026lt;strong\u0026gt;RealTime CTMS\u0026lt;/strong\u0026gt; or similar clinical trial management and billing systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Background in \u0026lt;strong\u0026gt;healthcare, clinical research, or clinical trial finance\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with \u0026lt;strong\u0026gt;clinical trial billing structures, sponsor contracts, and study-level financial reconciliation\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working in\u0026amp;nbsp;\u0026lt;strong\u0026gt;high-growth or multi-site organizations\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003490006,"name":"Finance \u0026 Accounting","child_ids":[],"parent_id":4003489006}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4653723006","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":4533823006,"location":{"name":"Cambridge, MA or New York, NY"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4653723006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"306","title":"Sr. Clinical Research Specialist ","company_name":"Iterative Health","first_published":"2026-02-13T10:52:48-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we are pioneering the application of powerful, proprietary artificial intelligence tools to the practice of cardiology and drug development.\u0026amp;nbsp; We’ve set out to drastically improve clinical decision-making while meaningfully improving patient lives through better diagnosis, disease management, and treatment, leading to better health outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the Senior Clinical Research Specialist I, you will report to the Head of Cardiology and Growth and work closely with the Director of Clinical Research (Cardiology), and work to integrate Iterative Health (IH) services and AI solutions at cardiology-based, clinical research sites throughout the US. This external-facing role will require strong communication, customer engagement and deep expertise in clinical research, in addition to a strong strategic skill set.\u0026amp;nbsp; You’ll work directly with your portfolio of sites by using our standard methodology to assess their\u0026amp;nbsp; current state. You’ll then work with your assigned sites to deliver customized training and day-to-day support that encourages research best practices, drives the adoption of IH services and products, and ensures our sites achieve their research goals.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Responsibilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate advanced knowledge of clinical research processes and tools, such as CTMS, pre-screening, and/or feasibility, and enhance these processes and outputs to effectively support our sites or internal teams.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a subject matter expert on clinical research workflows, in line with specific requirements of each protocol, optimized with Iterative\u0026amp;nbsp; Health (IH) services and AI solutions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage customer relationships with a high degree of professionalism and expertise ensuring timely responses, escalations of site issues, and building trust needed to help sites achieve IH goals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage IH solutions and services to help build best practice research sites, accelerate clinical trials, and build capacity at IH sites to execute high-quality clinical trials.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver customized training for different clinical research user groups and devise process\u0026amp;nbsp; maps/workflows, tools, and techniques to help sites incorporate IH services\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel to customer sites to support study site activation, drive patient screening, and\u0026amp;nbsp; standby support for randomization activities\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collect, analyze, and communicate the voice of IH customer successes, concerns, and\u0026amp;nbsp; product adoption issues/competency gaps and collaborate with IH cross-functional teams to\u0026amp;nbsp; design and deliver solutions\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor personal and site goals and KPIs and flag areas where additional support or assistance is needed\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Required skills:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BS/BA or higher degree.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 4 years of clinical research coordinator experience.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At least 8 years of experience with phase 2-4 pharma-sponsored clinical trials, including\u0026amp;nbsp; study start-up, CDA, feasibility, regulatory/standard operating procedures, study\u0026amp;nbsp; protocols, and regulations governing clinical research\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience coordinating, evaluating, and following patients’ participation through clinical trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent in the use of Microsoft Office/Google Apps products.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to navigate ambiguity and willingness to be flexible/adapt to changing work environments.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Desire to work with new tools and technology.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately. ● Willingness to travel to customer sites (~30%)\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Preferred skills:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ years as a Clinical Research Coordinator (CRC) working with cardiology trials or equivalent experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;General understanding of the evaluation and diagnosis of common cardiac disorders and diseases.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$85,000\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;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4025810006,"name":"210020 - Growth","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4666587006","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":4540430006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4666587006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"335","title":"Staff Data Engineer","company_name":"Iterative Health","first_published":"2026-04-24T16:03:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Accelerating clinical research is one of the defining challenges in healthcare. Promising therapies exist that patients can\u0026#39;t access because the operational infrastructure to run clinical trials efficiently doesn\u0026#39;t exist yet. We\u0026#39;re building it. That means designing technology systems that bring order to a fragmented landscape of clinical data sources, automating the operational work that slows trials down, and turning real-world clinical data into a foundation for predictive intelligence.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We\u0026#39;re building a uniquely valuable data asset: real-world patient and research data flowing across 80+ trial sites, spanning dozens of EHRs and clinical systems, focused on patient populations that are chronically underserved by existing clinical research infrastructure. Your job is to build the pipelines, data models, and AI infrastructure that make this asset real, from ingestion and normalization through to the systems that power predictions on top of it. You\u0026#39;ll own data quality and observability as foundational engineering problems. You\u0026#39;ll also have a direct hand in shaping how this data drives our AI strategy, what we model, what we predict, and what becomes possible.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is an opportunity for someone who wants to be part of a small, fast-moving engineering team at a formative stage. You\u0026#39;ll shape what gets built, how decisions get made, and what the team becomes.\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;Own the data layer and architecture:\u0026amp;nbsp; the models, schemas, and infrastructure decisions that everything downstream depends on\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and operate the pipelines and transformations that move data from ingestion through normalization, enrichment, and into the formats that support analytics, ML training, and production model serving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own data quality and observability: build the systems that make data issues visible and correctable before they compound\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with ML and engineering teams to identify what\u0026#39;s modelable, define training data requirements, and build the data foundations for new predictive capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define how clinical and operational data is governed across the system\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and select the tools and technologies that make up the data stack, with a clear point of view on build vs. buy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help shape the engineering culture of a small, growing team: how technical decisions get made, how problems get debated, what rigor looks like in practice\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience in data engineering or related roles, with significant time spent building data systems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with healthcare data strongly preferred (HL7, FHIR, claims, EHR extracts) or other complex, regulated data domains\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep experience modeling and integrating data from multiple heterogeneous sources with inconsistent schemas and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience applying AI and LLMs to data engineering problems: extraction, normalization, classification, entity resolution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of how data infrastructure supports ML workflows from feature engineering to training data pipelines to model serving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent in SQL and at least one modern programming language (Python, Java, Scala, Go), with experience across modern data infrastructure - distributed processing, streaming, cloud-native storage, orchestration, and transformation frameworks\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have built data systems from early stages, making foundational decisions with incomplete information\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Naturally raise the quality of the engineering around you through code review, design guidance, and honest technical conversation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience building data infrastructure that directly supports ML model training and evaluation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical trial operations, EDC systems, or life sciences data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;SOC 2, HIPAA or similar compliance experience baked into engineering practice\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A track record of building or improving data systems that others had given up on making reliable\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$200,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$325,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003470006,"name":"Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4666589006","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":4540431006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4666589006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"336","title":"Staff Data Scientist","company_name":"Iterative Health","first_published":"2026-04-24T16:03:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Accelerating clinical research is one of the defining challenges in healthcare. Promising therapies exist that patients can\u0026#39;t access because the operational infrastructure to run clinical trials efficiently doesn\u0026#39;t exist yet. We\u0026#39;re building it. That means designing technology systems that bring order to a fragmented landscape of clinical data sources, automating the operational work that slows trials down, and turning real-world clinical data into a foundation for predictive intelligence.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We\u0026#39;re looking for a Staff Data Scientist to be the person who understands our data deeply enough to know what\u0026#39;s possible and curious enough to prove it. We have a truly unique data set within the industry, connecting clinical data (emr, endoscopic video, etc…) to trial data across 80+ trial sites. We\u0026#39;re looking for someone who wants to dig deeply into this data - to understand its structure, its gaps, what it can tell us - and connect that understanding to real outcomes for sites and patients. The landscape is evolving rapidly, and the right person will have a point of view on how to apply new capabilities to our specific data and problems as they emerge.You\u0026#39;ll work hands-on with the data, structure experiments, evaluate what\u0026#39;s modelable, and directly influence what we build and how. This role sits at the intersection of data science, product strategy, and ML: you\u0026#39;ll lay the foundation for our predictive capabilities and shape what that function becomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is an opportunity for someone who wants to be part of a small, fast-moving engineering team at a formative stage. You\u0026#39;ll shape what gets built, how decisions get made, and what the team becomes.\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;Work with clinical, video, and clinical trial operational data to understand what\u0026#39;s there, what\u0026#39;s meaningful, and how we can use it to drive a more efficient clinical trial system\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and run experiments that determine what\u0026#39;s worth building\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay close to the evolving ML and model landscape and bring a point of view on how new capabilities apply to our data and problems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define the path from raw data to product and operationalization: what to model, how to evaluate it, and when it\u0026#39;s ready to ship\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with product and engineering to translate findings into concrete product decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities where our data creates unique predictive advantages\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate where we should build, where we should partner, and where existing approaches fall short\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help shape the engineering culture of a small, growing team: how technical decisions get made, how problems get debated, what rigor looks like in practice\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ years of experience in data science, applied ML, or quantitative research, with significant time spent hands-on with data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with healthcare data, clinical research, or life sciences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A deep curiosity to understand data and connect it to the real world\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep experience designing and running experiments: you know how to structure a question, test it honestly, and draw conclusions that hold up\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong statistical foundations and the judgment to know when a result is meaningful versus interesting\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Fluent in Python and SQL, comfortable working across the data stack from exploratory analysis through to production-ready pipelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working across data science, product, and engineering: you can influence what gets built, not just analyze what exists\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have worked with complex, messy, real-world data and know how to make it useful without pretending it\u0026#39;s clean\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledgeable about ML capabilities and frameworks, with the judgment to know when something is genuinely applicable versus hype\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Can communicate findings clearly to technical and non-technical audiences, and make a persuasive case for what to build next\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience working at growth stage startups (strongly preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with medical imaging or video data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical trial operations, disease classification, or patient identification problems\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building or defining the roadmap for an ML function from early stages\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A track record of data science work that directly changed product direction\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$200,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$325,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003470006,"name":"Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4666585006","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":4540429006,"location":{"name":"Cambridge, Massachusetts, United States, New York, New York, United States"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":null,"value_type":"single_select"}],"id":4666585006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"334","title":"Staff Software Engineer","company_name":"Iterative Health","first_published":"2026-04-24T16:04:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;About the Role\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Accelerating clinical research is one of the defining challenges in healthcare. Promising therapies exist that patients can\u0026#39;t access because the operational infrastructure to run clinical trials efficiently doesn\u0026#39;t exist yet. We\u0026#39;re building it. That means designing technology systems that bring order to a fragmented landscape of clinical data sources, automating the operational work that slows trials down, and turning real-world clinical data into a foundation for predictive intelligence.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We\u0026#39;re looking for a Staff Software Engineer to own the design and implementation of the core systems that make this possible. This means building robust integrations across a complex, fragmented landscape of EHRs, CTMS platforms, and clinical data sources, each with its own data models, access patterns, and operational constraints. It also means building the data infrastructure that powers our predictive capabilities: the pipelines, feature stores, and training infrastructure that allow us to move from raw clinical data to models that meaningfully improve trial execution. This is a generalist role for someone who thinks in systems. You\u0026#39;ll move between architecture and implementation, between integration engineering and ML infrastructure, between defining technical strategy and writing the code that proves it out. The problems are genuinely hard, largely unsolved, and what you build will matter.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is an opportunity for someone who wants to be a part of a small, fast moving engineering team at a formative stage. You\u0026#39;ll shape what gets built, how decisions get made, and what the team becomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\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;Own the technical architecture for our core systems and build the foundational abstractions and interfaces that everything else is built on top of\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build reliable integrations with dozens of external clinical data systems (EHRs, CTMS, eSource, labs), treating this as a hard systems design problem, not just an ingestion problem\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and evolve the infrastructure that supports model training and predictive capabilities, from ingestion through feature engineering and serving\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Move fast by prototyping to drive experimentation; derisk ideas quickly to keep the team building what works\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and choose the technologies we build on: make build vs. buy decisions, select vendors, and shape our long-term infrastructure strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Make the key technical tradeoffs between speed and durability, between generality and shipping\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work across product, clinical operations, and data science to make sure you\u0026#39;re solving the right problems, not just the interesting ones\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help shape the engineering culture of a small, growing team: how technical decisions get made, how problems get debated, what rigor looks like in practice\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;What We’re Looking For\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Required Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Have 10+ years of software engineering experience, with significant time spent designing and building systems not just features\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with healthcare data systems (HL7, FHIR, EHR/EMR integrations) or other highly regulated data environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have 2+ years experience working in a high-growth startup environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have deep experience with system integration, particularly across unreliable or heterogeneous external data sources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Can think through and explain the full picture of a complex system while still being effective at the implementation level\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience using AI tooling and frameworks as part of your engineering workflow\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have built data pipelines and infrastructure that support analytical or ML workloads in production\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong across the backend stack (Python, SQL, cloud infrastructure) and can pick up new tools and systems quickly\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Have built systems from early stages, making foundational decisions with incomplete information, not just extending established infrastructure\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Naturally raise the quality of the engineering around you through code review, architecture guidance, and honest technical conversation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Preferred Qualifications\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Experience building ML training infrastructure or feature platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical operations, systems, or life sciences data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;SOC 2, HIPAA or similar compliance experience baked into engineering practice\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A track record of building systems that had to work correctly under real operational constraints, scale and complexity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\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;New York pay range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$200,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$325,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4003470006,"name":"Engineering","child_ids":[],"parent_id":null}],"offices":[{"id":4001631006,"name":"Cambridge HQ","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null},{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/iterativehealth/jobs/4683541006","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":4548752006,"location":{"name":"NYC HQ"},"metadata":[{"id":17013918006,"name":"Job Family","value":null,"value_type":"single_select"},{"id":17012825006,"name":"In Person, Hybrid or Remote","value":"Hybrid","value_type":"single_select"}],"id":4683541006,"updated_at":"2026-06-04T15:39:11-04:00","requisition_id":"394","title":"Talent Acquisition Sourcing Specialist","company_name":"Iterative Health","first_published":"2026-05-21T15:32:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://iterative.health/?utm_source=chatgpt.com\u0026quot;\u0026gt;Iterative Health\u0026lt;/a\u0026gt;, is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors\u0026#39; scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Why This Role Matters\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;As Iterative Health continues to scale, we are seeking a proactive and relationship-driven Talent Acquisition Sourcer to help build and engage high-quality talent pipelines across the organization. This role will play a critical part in supporting the company’s long-term hiring strategy by identifying, attracting, and nurturing talent across clinical research, operations and corporate.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;This is an ideal opportunity for someone who is passionate about networking, relationship-building, employer branding, and creating meaningful candidate connections within the healthcare, clinical research, and technology space. You will help strengthen Iterative Health’s presence in the market while building pipelines that support both immediate and future talent needs.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Where You’ll Drive Impact\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\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;Build and maintain proactive talent pipelines across operations and clinical research functions to support current and future hiring needs\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Develop and execute innovative sourcing strategies to identify and engage top talent in competitive markets\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Act as a brand ambassador for Iterative Health by creating meaningful candidate connections and delivering a positive candidate experience throughout the sourcing and engagement process\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Partner closely with Talent Acquisition Partners and TA leadership teams to align sourcing strategies with business priorities and workforce planning needs\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Build relationships within the healthcare, clinical research, biotech, and health tech communities through networking, industry associations, conferences, and events\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Lead and support employer branding initiatives across platforms including LinkedIn, Glassdoor, Indeed, and other talent channels to strengthen Iterative Health’s market presence and candidate engagement\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Manage job board strategy to support effective talent attraction efforts\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Represent Iterative Health at recruitment events, networking events, industry conferences, career fairs, and association events to build brand awareness and cultivate strong talent communities\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Help build and activate Iterative Health’s Employer Value Proposition in partnership with Marketing and cross-functional teams\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Host and attend recruiting and networking events and conferences\u0026amp;nbsp; that support talent engagement, pipeline development, and employer brand visibility\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Leverage sourcing tools, recruiting technologies, market insights, and talent intelligence to identify and attract diverse, high-quality talent\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Maintain strong engagement with passive candidates and cultivate long-term relationships within key talent communities\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Partner with the Talent Acquisition team to continuously improve sourcing strategies, candidate outreach, and talent engagement practices\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Track sourcing activity, pipeline health, and recruiting metrics to support data-driven decision-making and continuous improvement\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Stay informed on industry trends, competitive talent landscapes, and emerging recruiting best practices\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Collaborate cross-functionally with Marketing on talent attraction initiatives and recruiting projects\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Support additional talent initiatives and responsibilities that align with organizational growth and evolving business needs\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;How We Work\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\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;Collaborative and low-ego team environment\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Fast-moving and highly iterative culture\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Strong focus on ownership and accountability\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Mission-driven and patient-centered mindset\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Open communication and continuous learning\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Comfortable navigating evolving business needs\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;What You Bring to the Team\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;3+ years of sourcing, recruiting, talent acquisition, or talent engagement experience\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Experience building talent pipelines and sourcing passive candidates across multiple functions\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Strong networking and relationship-building skills with the ability to engage candidates and industry professionals authentically\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Experience utilizing LinkedIn Recruiter, sourcing platforms, talent communities, and recruiting tools\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Passion for employer branding, talent engagement, and candidate experience\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Strong communication and organizational skills with attention to detail and follow-through\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Ability to manage multiple priorities in a fast-paced, growth-oriented environment\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Resourceful, proactive, and solutions-oriented mindset\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Experience supporting healthcare, biotech, clinical research, health tech, or high-growth organizations is strongly preferred\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Experience with Greenhouse or similar ATS platforms is preferred\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h4\u0026gt;\u0026amp;nbsp;\u0026lt;/h4\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits That Support You\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;We believe great teams do their best work when they feel supported — professionally and personally.\u0026lt;/span\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;Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Mental health and wellness support through Spring Health\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;401(k) program with a company match of up to 3% (up to $3,000 annually)\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Weekly in-office lunch benefit every Tuesday\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;100% company-paid short-term and long-term disability coverage\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;Annual wellness and professional development stipend to support your health and growth\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;And more!\u0026lt;/span\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h2\u0026gt;\u0026lt;span style=\u0026quot;font-size: 12pt;\u0026quot;\u0026gt;At Iterative Health, we believe great talent drives innovation. If you’re excited about helping transform the future of clinical research, we encourage you to apply.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/h2\u0026gt;\n\u0026lt;h4\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/h4\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;New York 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;$110,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4027138006,"name":"645000 - Talent Acquisition ","child_ids":[],"parent_id":null}],"offices":[{"id":4012942006,"name":"NYC HQ","location":"New York, New York, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":44}}