{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4402918009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4233101009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4402918009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"132","title":"Associate Corporate Counsel, Contracts","company_name":"Beeline Medicines","first_published":"2026-09-10T18:39:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Corporate Counsel, Contracts, provides legal support for the drafting, review, and negotiation of a broad range of commercial agreements, ensuring contracts appropriately protect company interests and comply with applicable laws and internal policies. Partners closely with Procurement, R\u0026amp;amp;D, and other business functions to keep contracting moving at the pace the business needs, while maintaining and improving templates, playbooks, and negotiation guidelines that scale legal support across the organization. Advises internal stakeholders on contractual risk and obligations, escalating higher-risk or novel issues to senior legal leadership as appropriate. This role is well suited to a contracts attorney who enjoys high-volume, fast-paced transactional work in a growing life sciences company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Draft, review, and negotiate a variety of commercial agreements, including CDAs, MSAs, CRO/vendor agreements, and consulting agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Procurement, R\u0026amp;amp;D, and other business functions to support contracting needs and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and improve contract templates, playbooks, and negotiation guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise internal stakeholders on contractual risk, obligations, and compliance considerations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the contract lifecycle management system, ensuring accurate tracking and record-keeping.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with due diligence and contract review for business development and licensing transactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Escalate higher-risk or novel contract issues to senior legal leadership as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;JD from an accredited law school required; active bar membership in good standing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of relevant contracts/transactional experience, in-house or at a law firm, ideally within the life sciences industry preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of commercial contract law and life sciences-specific agreement types (CDA, MSA, clinical trial agreements) with familiarity with contract lifecycle management systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of intellectual property and confidentiality considerations in commercial agreements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of key risk allocation and indemnification concepts in vendor and CRO contracts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work independently while knowing when to escalate risk to senior counsel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment prioritizing a high volume of concurrent contracting requests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to drive process improvements in templates and playbooks that scale legal support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong drafting, negotiation, and client-counseling communication skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to clearly explain contractual risk and options to non-legal business stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at building relationships across Procurement, R\u0026amp;amp;D, and other business functions.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$181,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$235,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035455009,"name":"Legal","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4402875009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4233092009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4402875009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"131","title":"Associate Director, Biostatistics","company_name":"Beeline Medicines","first_published":"2026-09-10T18:26:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Biostatistics provides statistical leadership for assigned clinical development programs, including study design, analysis planning, and statistical reporting in support of clinical trial execution and regulatory submissions. Serves as the lead statistician on cross-functional study teams, shaping protocol design, sample size and power considerations, and analysis strategy from early development through submission. Oversees the quality and timeliness of statistical deliverables, whether produced internally or through CRO partners, and ensures all outputs meet ICH and regulatory expectations. This role requires both deep statistical expertise and the ability to communicate complex quantitative concepts clearly to clinical, regulatory, and executive audiences.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as\u0026amp;nbsp;\u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as lead statistician for one or more clinical studies, from protocol design through clinical study report.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop statistical analysis plans (SAPs), sample size/power calculations, and randomization schemes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee production and QC of tables, listings, and figures (TLFs) performed internally or by CROs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Clinical, Regulatory, and Data Management on study design, protocol development, and data review.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute statistical input to regulatory submissions, briefing documents, and health authority responses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and provide statistical input on clinical study reports and publications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure statistical deliverables comply with ICH guidelines and applicable regulatory standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;PhD in Biostatistics, Statistics, or a closely related quantitative discipline required.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of biostatistics experience in pharmaceutical, biotechnology, and/or CRO settings preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology, inflammation, or a related therapeutic area preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced proficiency in SAS and/or R for statistical analysis and programming.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of clinical trial design and operation, ICH E9 principles, and CDISC ADaM standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with adaptive trial designs, interim analyses, and Bayesian or frequentist methods as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with CRO statistical oversight and governance — including statistical deliverable review, CRO quality management, and the establishment of biostatistics standards within a virtual or outsourced development model.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to lead statistical strategy discussions with cross-functional and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound scientific judgment in interpreting and communicating complex statistical results.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to translate statistical concepts for non-statistician audiences, including regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at presenting statistical findings to program teams and senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at collaborating cross-functionally with Clinical, Regulatory, and Data Management colleagues.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$181,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$235,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035445009,"name":"Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4439186009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4256622009,"location":{"name":"United States"},"metadata":null,"id":4439186009,"updated_at":"2026-10-08T15:54:40-04:00","requisition_id":"152","title":"Associate Director, Clinical Data Management","company_name":"Beeline Medicines","first_published":"2026-10-08T15:54:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Clinical Data Management Leads clinical data management activities across one or more clinical programs, ensuring the timely delivery of high-quality, audit-ready clinical trial data in support of regulatory submissions and clinical development timelines. Acts as the primary data management point of contact for assigned programs, overseeing CRO and vendor performance, database design, and data cleaning strategy from study start-up through database lock. Partners closely with Biostatistics, Statistical Programming, Clinical Operations, Clinical Development, Pharmacovigilance and Quality to ensure data management deliverables align with study milestones, data quality objectives and inspection-readiness standards. This role combines deep technical data management expertise with the leadership skills needed to guide cross-functional teams and external vendors toward consistent, high-quality outcomes. This role reports to the Director, Clinical Data Management.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Remote -\u0026amp;nbsp;\u0026lt;/strong\u0026gt;This position is designated as remote; the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company\u0026#39;s discretion based on business need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee the development and review of key data management study documents such as Data Management Plans, CRF/eCRF design specifications, data validation plans, custom listings/reports, and data cleaning plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee EDC and other clinical data systems build in support of protocol objectives, site-level and patient-level data entry workflows, user acceptance testing (UAT), database releases, mid-study updates, interim snapshots and database lock activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor clinical data quality, study metrics and KPIs to ensure timely and accurate data cleaning, discrepancy management, medical coding (MedDRA, WHO Drug), and reconciliation of external data sources (e.g., central labs, eCOA, safety data).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to internal and external cross-functional study team meetings by communicating study status, proactively identifying risks to timelines, data quality, and regulatory compliance, and recommending mitigation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all data management activities comply with ICH E6(R3) GCP guidelines, 21 CFR Parts 11 and 312, data security, privacy (e.g., GDPR, HIPAA) and other applicable global regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to process improvement initiatives, SOP development, and data management standards across programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of CDISC standards CDASH/SDTM, statistical analysis dataset specifications, and submission-ready data packages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation for regulatory inspections and audits by maintaining complete documentation of data management activities and sponsor oversight and ensure regular documentation filings into the Trial Master File.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Bachelor’s degree in Life Sciences, Health Sciences, Computer Science, or a related discipline, or equivalent education and experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 7 years of progressive experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology or autoimmune therapeutic areas preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience managing CDM activities across all phases of clinical development (Phase I–III), including late-stage and/or registration-enabling trials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience managing CRO relationships and overseeing outsourced CDM activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with EDC platforms (e.g., Medidata Rave, Veeva Vault EDC) and CDISC (CDASH/SDTM/ADaM) standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of data cleaning, query management, and database lock processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in medical coding dictionaries (MedDRA, WHO Drug) and coding conventions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with centralized data review methodologies such as data visualizations and review tools for identifying data quality trends and leveraging risk-based monitoring (RBM) approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to lead cross-functional study teams and manage CRO performance without direct reporting authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication for cross-functional and vendor collaboration.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to present data management status and risks to program leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at translating technical data issues into clear, actionable summaries for non-DM stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at facilitating technical system design discussions and data quality oversight review meetings with internal and external cross-functional team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 15%+ as needed of time or more including occasional overnight stay driven by business need\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$181,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$235,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035445009,"name":"Biometrics","child_ids":[],"parent_id":null}],"offices":[{"id":4036151009,"name":"Remote (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4371396009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4214650009,"location":{"name":"Stamford, Connecticut, United States"},"metadata":null,"id":4371396009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"105","title":"Associate Director, Financial Systems Service Delivery","company_name":"Beeline Medicines","first_published":"2026-08-16T14:40:58-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Financial Systems Service Delivery is responsible for the strategic management, optimization, and ongoing service delivery of the organization\u0026#39;s financial systems and technology infrastructure — with NetSuite serving as the core ERP platform — including NetSuite financial reporting and analytics, expense management systems, and related finance technology applications. This role sits at the intersection of finance and technology, serving as the primary owner and lead administrator of the NetSuite environment and the key liaison between Finance, IT, NetSuite (Oracle), and external implementation partners. The Associate Director ensures that NetSuite and connected financial systems are configured, maintained, and continuously improved to support accurate financial reporting, scalable accounting operations, and strong internal controls. Beyond system administration, this individual is responsible for delivering a high standard of financial systems service to internal Finance users — establishing support processes, training frameworks, and governance models that enable the Finance team to operate with efficiency, confidence, and data integrity across all platforms.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and administer the organization\u0026#39;s NetSuite ERP environment as the system of record — including core financials, subsidiary/OneWorld structure, segments and classifications, SuiteApps, and integrated finance applications (financial reporting, expense management, procurement) — ensuring all systems are properly configured, maintained, and operating at peak performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the financial systems service delivery function — establishing and managing user support processes, NetSuite role and permission governance, issue resolution workflows, and service level standards that ensure Finance team members receive timely, effective support across all platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement of NetSuite and connected systems — leveraging SuiteFlow workflows, SuiteScript customizations, saved searches, and SuiteAnalytics to automate manual processes, enhance configurations, improve reporting capabilities, and optimize workflows that improve the efficiency and accuracy of accounting and finance operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage user provisioning across all financial systems, facilitating appropriate segregation of duties, ensuring appropriate approvals and documentation to support SOX compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate NetSuite implementations, module rollouts, and enhancements, and govern the twice-yearly NetSuite release cycle — leading project planning, requirements gathering, sandbox configuration, regression and user acceptance testing (UAT), and go-live support for all financial technology projects in partnership with IT and external NetSuite partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain a robust financial systems controls environment — designing and enforcing NetSuite role-based access controls, segregation of duties frameworks, audit trail and change management practices, and IT general controls (ITGCs) that support SOX compliance and internal audit requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary point of contact and relationship manager for NetSuite (Oracle), SuiteApp providers, and implementation partners — managing contracts, license and user counts, service level agreements, product roadmaps, and support escalations to ensure vendor performance and platform reliability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and deliver NetSuite training programs and documentation — developing user guides, training materials, and onboarding resources that enable Finance team members to use financial systems effectively and consistently across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Bachelor\u0026#39;s degree in Accounting, Finance, Information Systems, or a related field required. Master\u0026#39;s degree or MBA is a plus. NetSuite certification (SuiteFoundation, Certified Administrator, or Certified ERP Consultant) strongly preferred; CPA or CMA is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8 years of progressive experience in financial systems administration, ERP management, or finance technology roles, with at least 3–5 years in a senior or lead capacity administering NetSuite preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with NetSuite implementation, configuration, and optimization required — including core financials, saved searches and reporting, SuiteFlow, and role/permission design. Experience with NetSuite OneWorld, Advanced Revenue Management, SuiteBilling, or Fixed Assets Management is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a life sciences, biotech, or pharmaceutical environment preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in NetSuite administration and configuration — including chart of accounts and segment design, subsidiary/OneWorld setup, financial report and saved search building, SuiteFlow workflow automation, SuiteScript customization oversight, form and field customization, and role-based user access management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of financial systems controls within NetSuite — including IT general controls (ITGCs), segregation of duties frameworks, role and permission governance, audit trail monitoring, and sandbox-to-production change management applicable to SOX-compliant environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in financial reporting and BI tools — including NetSuite SuiteAnalytics, Analytics Workbook, and the SuiteAnalytics Connect / ODBC data source, along with Tableau or Power BI — with experience building and maintaining financial dashboards, automated reports, and self-service reporting environments for Finance users.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project management capabilities — demonstrated track record of leading NetSuite implementations, module rollouts, and finance technology projects on time and within scope, managing competing priorities and cross-functional stakeholders effectively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative cross-functional partner — builds productive working relationships with Finance, IT, Internal Audit, and external NetSuite partners; effectively bridges the language gap between technical system capabilities and Finance operational requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective technical communicator — able to translate complex NetSuite configurations, ITGC requirements, and financial technology concepts into clear, accessible language for Finance users, IT partners, and executive stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in developing user-facing NetSuite training materials, system documentation, and process guides that improve Finance team self-sufficiency and reduce reliance on manual workarounds.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong vendor relationship communicator — manages external vendor relationships with clarity, accountability, and professionalism; articulates system requirements, escalates issues effectively, and holds partners to documented service commitments.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$165,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$214,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035459009,"name":"Accounting","child_ids":[],"parent_id":null}],"offices":[{"id":4034862009,"name":"Stamford, CT Office","location":"Stamford, Connecticut, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4398898009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4231020009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4398898009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"126","title":"Associate Director, Scientific Communications","company_name":"Beeline Medicines","first_published":"2026-09-08T22:29:52-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director of Scientific Communications will support the development and execution of the scientific communications strategy across the portfolio, leading day-to-day publication planning, congress activities, and scientific content development. This individual partners closely with the Senior Director, Scientific Communications and cross-functional stakeholders in Clinical Development, Regulatory, Medical Affairs, and Commercial to translate clinical and translational data into clear, compliant, and scientifically rigorous materials for internal and external audiences. The role requires strong scientific writing ability, project management skills, and comfort operating in a fast-paced, evolving biotech environment\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support development and lead execution of the scientific communications plan in alignment with asset strategy and medical affairs objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage global publication activities (author engagement, abstracts, manuscripts, posters, oral presentations) in compliance with GPP2022 and company SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the execution of plans for major international and regional medical meetings, including content development and internal alignment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Draft and edit scientific content, including slide decks, scientific exchange materials, FAQs, and training resources for Field Medical teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional teams to ensure accurate interpretation and timely dissemination of data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain publication trackers, timelines, and vendor/agency relationships to ensure on-time, on-budget delivery\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support advisory boards, investigator meetings, and external scientific forums\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in establishing processes and standards to ensure consistency and compliance across scientific materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;PhD, PharmD, MS, or equivalent advanced scientific degree required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of experience in scientific communications, medical affairs, or related roles within biotech or pharmaceutical industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting publication strategy and congress execution, ideally for late-stage (Phase 2/3 or Phase 3) programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in autoimmune, immunology, or inflammatory diseases preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of scientific publication standards, data disclosure requirements, and medical compliance, including GPP2022 and ICMJE guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent project management and organizational skills, with ability to manage multiple concurrent timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to a culture of scientific excellence, accountability, and continuous improvement within the scientific communications function\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build credibility with cross-functional partners across Clinical Development, Regulatory, Commercial, and Medical Affairs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exercise sound judgment and independent problem-solving in a fast-paced, resource-constrained environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate complex clinical and scientific data into clear, audience-appropriate narratives for diverse stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate proactively with cross-functional partners on publication timelines, congress deliverables, and project status\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistency, accuracy, and compliance of scientific messaging across all channels and materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate effectively with clinical, regulatory, and commercial colleagues to align on scientific narrative\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$165,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$214,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4391884009","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":4227046009,"location":{"name":"Brazil"},"metadata":null,"id":4391884009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"114","title":"Clinical Engagement Lead - Brazil","company_name":"Beeline Medicines","first_published":"2026-09-01T17:50:41-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Engagement Lead, is a field-based is a senior level, site facing clinical development professional responsible for building and managing investigator and site relationships across the globe in support of the organization\u0026#39;s clinical trial portfolio. This role serves as the primary site-facing liaison between the organization and its global clinical investigators, academic medical centers, and research sites — supporting site identification, investigator engagement, and clinical trial execution to position the organization’s I\u0026amp;amp;I programs competitively in the clinical research landscape. The Clinical Engagement Lead combines knowledge of the I\u0026amp;amp;I therapeutic area with strong relationship management skills and a thorough understanding of clinical trial operations — serving as a trusted partner to investigators and a critical field intelligence link back to the internal Clinical Development and Medical Affairs teams. This is a highly visible, externally focused role that requires the ability to represent the organization’s science with authority, build lasting relationships with leading clinical researchers, and operate independently across a broad assigned geography.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Brazil and other LATAM countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and manage a portfolio of region/country investigator and clinical site relationships in the I\u0026amp;amp;I therapeutic area — identifying, engaging, and developing long-term partnerships with principal investigators, academic medical centers, community research sites, and subspecialty practices relevant to Beeline\u0026#39;s clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead site identification and feasibility activities for clinical trials — conducting operational site assessments, evaluating investigator interest and patient population access, and providing strategic recommendations to Clinical Development and Clinical Operations on site selection and activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary clinical liaison to regional/country level investigators — facilitating peer-to-peer scientific exchange on Beeline\u0026#39;s pipeline, conducting protocol discussions, supporting site initiation and training, and maintaining ongoing engagement with investigators throughout the trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial enrollment and retention at region/country sites — working proactively with investigators and site staff to identify enrollment challenges, implement site-level solutions, and maintain site motivation and engagement across all active Beeline studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capture and communicate region/country clinical landscape intelligence — including investigator perspectives, competitive trial activity, site capacity trends, and unmet medical need insights — back to Clinical Development, Medical Affairs, and Commercial teams in a structured, actionable manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs MSLs to ensure coordination and alignment of scientific engagement activities at the investigator level — establishing clear boundaries between clinical trial support and medical affairs activities and collaborating to maximize the impact of both.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent organization clinical and scientific meetings, investigator symposia, disease-area conferences, and site visits — engaging with the clinical research community as a credible, knowledgeable, and trusted organizational representative.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement site engagement strategies to improve study start-up, enrollment performance, retention, and site satisfaction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with investigators, study coordinators, and site staff to support patient identification and recruitment efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational guidance and best practices to sites related to diverse patient enrollment and community engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct regular field engagement with investigative sites and community stakeholders to strengthen study execution and recruitment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor enrollment trends, site performance metrics, and patient engagement effectiveness using data-driven approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify enrollment risks proactively and implement mitigation and recovery plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelors degree in scientific or related discipline required. Advanced degree preferred—MS or MPH in a relevant clinical, biomedical, or pharmaceutical sciences discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in clinical development, clinical research, clinical operations, or a field-based clinical engagement role within the pharmaceutical or biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience managing investigator relationships and supporting clinical trial site activation and enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience collaborating with CROs, investigative sites, and field medical teams, including MSL partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific and clinical knowledge of immunology and inflammation — including disease biology, standard of care, clinical trial design considerations, and the competitive clinical research landscape across relevant I\u0026amp;amp;I indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in clinical trial site management and investigator engagement — including site feasibility assessment, investigator identification and qualification, site initiation support, and enrollment optimization strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GCP requirements, ICH guidelines, and FDA regulations governing investigator interactions, clinical site oversight, and field-based clinical development activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly self-directed field professional — manages a complex investigator portfolio independently, prioritizes site engagement activities strategically, and operates with minimal supervision across a broad geography.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relationship-driven and trusted clinical trial resource — builds genuine, long-term partnerships with investigators and site staff based on scientific credibility, reliability, and authentic commitment to supporting research excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive field intelligence contributor — consistently translates field observations into actionable insights that improve program strategy, site selection, and enrollment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035447009,"name":"Clinical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4054779009,"name":"Brazil","location":"Brazil","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4391870009","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":4227040009,"location":{"name":"India"},"metadata":null,"id":4391870009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"113","title":"Clinical Engagement Lead - India","company_name":"Beeline Medicines","first_published":"2026-09-01T17:46:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Engagement Lead, is a field-based is a senior level, site facing clinical development professional responsible for building and managing investigator and site relationships across the globe in support of the organization\u0026#39;s clinical trial portfolio. This role serves as the primary site-facing liaison between the organization and its global clinical investigators, academic medical centers, and research sites — supporting site identification, investigator engagement, and clinical trial execution to position the organization’s I\u0026amp;amp;I programs competitively in the clinical research landscape. The Clinical Engagement Lead combines knowledge of the I\u0026amp;amp;I therapeutic area with strong relationship management skills and a thorough understanding of clinical trial operations — serving as a trusted partner to investigators and a critical field intelligence link back to the internal Clinical Development and Medical Affairs teams. This is a highly visible, externally focused role that requires the ability to represent the organization’s science with authority, build lasting relationships with leading clinical researchers, and operate independently across a broad assigned geography.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;India and other APAC countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and manage a portfolio of region/country investigator and clinical site relationships in the I\u0026amp;amp;I therapeutic area — identifying, engaging, and developing long-term partnerships with principal investigators, academic medical centers, community research sites, and subspecialty practices relevant to Beeline\u0026#39;s clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead site identification and feasibility activities for clinical trials — conducting operational site assessments, evaluating investigator interest and patient population access, and providing strategic recommendations to Clinical Development and Clinical Operations on site selection and activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary clinical liaison to regional/country level investigators — facilitating peer-to-peer scientific exchange on Beeline\u0026#39;s pipeline, conducting protocol discussions, supporting site initiation and training, and maintaining ongoing engagement with investigators throughout the trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial enrollment and retention at region/country sites — working proactively with investigators and site staff to identify enrollment challenges, implement site-level solutions, and maintain site motivation and engagement across all active Beeline studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capture and communicate region/country clinical landscape intelligence — including investigator perspectives, competitive trial activity, site capacity trends, and unmet medical need insights — back to Clinical Development, Medical Affairs, and Commercial teams in a structured, actionable manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs MSLs to ensure coordination and alignment of scientific engagement activities at the investigator level — establishing clear boundaries between clinical trial support and medical affairs activities and collaborating to maximize the impact of both.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent organization clinical and scientific meetings, investigator symposia, disease-area conferences, and site visits — engaging with the clinical research community as a credible, knowledgeable, and trusted organizational representative.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement site engagement strategies to improve study start-up, enrollment performance, retention, and site satisfaction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with investigators, study coordinators, and site staff to support patient identification and recruitment efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational guidance and best practices to sites related to diverse patient enrollment and community engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct regular field engagement with investigative sites and community stakeholders to strengthen study execution and recruitment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor enrollment trends, site performance metrics, and patient engagement effectiveness using data-driven approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify enrollment risks proactively and implement mitigation and recovery plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelors degree in scientific or related discipline required. Advanced degree preferred—MS or MPH in a relevant clinical, biomedical, or pharmaceutical sciences discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in clinical development, clinical research, clinical operations, or a field-based clinical engagement role within the pharmaceutical or biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience managing investigator relationships and supporting clinical trial site activation and enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience collaborating with CROs, investigative sites, and field medical teams, including MSL partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific and clinical knowledge of immunology and inflammation — including disease biology, standard of care, clinical trial design considerations, and the competitive clinical research landscape across relevant I\u0026amp;amp;I indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in clinical trial site management and investigator engagement — including site feasibility assessment, investigator identification and qualification, site initiation support, and enrollment optimization strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GCP requirements, ICH guidelines, and FDA regulations governing investigator interactions, clinical site oversight, and field-based clinical development activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly self-directed field professional — manages a complex investigator portfolio independently, prioritizes site engagement activities strategically, and operates with minimal supervision across a broad geography.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relationship-driven and trusted clinical trial resource — builds genuine, long-term partnerships with investigators and site staff based on scientific credibility, reliability, and authentic commitment to supporting research excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive field intelligence contributor — consistently translates field observations into actionable insights that improve program strategy, site selection, and enrollment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035447009,"name":"Clinical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4076256009,"name":"India","location":"India","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4305462009","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":4179036009,"location":{"name":"Japan"},"metadata":null,"id":4305462009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"87","title":"Clinical Engagement Lead - Japan","company_name":"Beeline Medicines","first_published":"2026-07-02T17:39:19-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Engagement Lead, is a field-based is a senior level, site facing clinical development professional responsible for building and managing investigator and site relationships across the globe in support of the organization\u0026#39;s clinical trial portfolio. This role serves as the primary site-facing liaison between the organization and its global clinical investigators, academic medical centers, and research sites — supporting site identification, investigator engagement, and clinical trial execution to position the organization’s I\u0026amp;amp;I programs competitively in the clinical research landscape. The Clinical Engagement Lead combines knowledge of the I\u0026amp;amp;I therapeutic area with strong relationship management skills and a thorough understanding of clinical trial operations — serving as a trusted partner to investigators and a critical field intelligence link back to the internal Clinical Development and Medical Affairs teams. This is a highly visible, externally focused role that requires the ability to represent the organization’s science with authority, build lasting relationships with leading clinical researchers, and operate independently across a broad assigned geography.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Japan and other APAC countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and manage a portfolio of region/country investigator and clinical site relationships in the I\u0026amp;amp;I therapeutic area — identifying, engaging, and developing long-term partnerships with principal investigators, academic medical centers, community research sites, and subspecialty practices relevant to Beeline\u0026#39;s clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead site identification and feasibility activities for clinical trials — conducting operational site assessments, evaluating investigator interest and patient population access, and providing strategic recommendations to Clinical Development and Clinical Operations on site selection and activation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary clinical liaison to regional/country level investigators — facilitating peer-to-peer scientific exchange on Beeline\u0026#39;s pipeline, conducting protocol discussions, supporting site initiation and training, and maintaining ongoing engagement with investigators throughout the trial lifecycle.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial enrollment and retention at region/country sites — working proactively with investigators and site staff to identify enrollment challenges, implement site-level solutions, and maintain site motivation and engagement across all active Beeline studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Capture and communicate region/country clinical landscape intelligence — including investigator perspectives, competitive trial activity, site capacity trends, and unmet medical need insights — back to Clinical Development, Medical Affairs, and Commercial teams in a structured, actionable manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Medical Affairs MSLs to ensure coordination and alignment of scientific engagement activities at the investigator level — establishing clear boundaries between clinical trial support and medical affairs activities and collaborating to maximize the impact of both.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent organization clinical and scientific meetings, investigator symposia, disease-area conferences, and site visits — engaging with the clinical research community as a credible, knowledgeable, and trusted organizational representative.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement site engagement strategies to improve study start-up, enrollment performance, retention, and site satisfaction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with investigators, study coordinators, and site staff to support patient identification and recruitment efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational guidance and best practices to sites related to diverse patient enrollment and community engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct regular field engagement with investigative sites and community stakeholders to strengthen study execution and recruitment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor enrollment trends, site performance metrics, and patient engagement effectiveness using data-driven approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify enrollment risks proactively and implement mitigation and recovery plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelors degree in scientific or related discipline required. Advanced degree preferred—MS or MPH in a relevant clinical, biomedical, or pharmaceutical sciences discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in clinical development, clinical research, clinical operations, or a field-based clinical engagement role within the pharmaceutical or biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience managing investigator relationships and supporting clinical trial site activation and enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience collaborating with CROs, investigative sites, and field medical teams, including MSL partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific and clinical knowledge of immunology and inflammation — including disease biology, standard of care, clinical trial design considerations, and the competitive clinical research landscape across relevant I\u0026amp;amp;I indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in clinical trial site management and investigator engagement — including site feasibility assessment, investigator identification and qualification, site initiation support, and enrollment optimization strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of GCP requirements, ICH guidelines, and FDA regulations governing investigator interactions, clinical site oversight, and field-based clinical development activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly self-directed field professional — manages a complex investigator portfolio independently, prioritizes site engagement activities strategically, and operates with minimal supervision across a broad geography.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relationship-driven and trusted clinical trial resource — builds genuine, long-term partnerships with investigators and site staff based on scientific credibility, reliability, and authentic commitment to supporting research excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive field intelligence contributor — consistently translates field observations into actionable insights that improve program strategy, site selection, and enrollment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035447009,"name":"Clinical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4065331009,"name":"Japan","location":null,"child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4450953009","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":4266578009,"location":{"name":"United Kingdom"},"metadata":null,"id":4450953009,"updated_at":"2026-11-02T18:08:06-05:00","requisition_id":"155","title":"Clinical Engagement Regional Associate Director (Europe \u0026 Asia)","company_name":"Beeline Medicines","first_published":"2026-10-13T19:07:09-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Engagement Regional Associate Director is a field-based, senior level, people-management role responsible for leading a team of Clinical Engagement Leads (CELs) who are responsible for building and managing investigator and site relationships across the organization’s clinical trial portfolio. This role serves as the central global people manager for the field-based clinical engagement function in assigned region(s)execution of investigator and site relationship management across the assigned region/countries. The Clinical Engagement Manager combines people leadership skills with deep knowledge of the I\u0026amp;amp;I therapeutic area and clinical trial operations — serving as the escalation point for complex investigator and site issues and as the primary conduit of field intelligence and team performance to senior Clinical Development and Medical Affairs leadership. This is a highly visible role that requires the ability to build and lead a high-performing field team and operate independently across a broad assigned geography.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Europe \u0026amp;amp; Asia\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide day-to-day people leadership for a team of Clinical Engagement Leads — including coaching, performance management, goal-setting, and career development to build and sustain a high-performing field-based engagement team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support site engagement strategy and priorities for the assigned region/country — translating clinical program goals into team-level objectives for investigator identification, site feasibility, activation, and enrollment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Recruit, onboard, and develop Clinical Engagement Lead talent — partnering with HR and Clinical Operations leadership on hiring decisions, territory/portfolio assignments, and ongoing skills development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and approve site engagement plans and feasibility recommendations developed by the team, providing strategic input on site selection, activation timelines, and enrollment risk mitigation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the escalation point for complex investigator and site relationship issues, partnering with Clinical Operations, Clinical Development and Medical Affairs leadership to resolve challenges that exceed team-member authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Consolidate and communicate team-level field intelligence, enrollment trends, and performance metrics to senior Clinical Operations and Clinical Development and Medical Affairs leadership in a structured, actionable manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with cross-functional leaders in Clinical Development, Medical Affairs, and HR to ensure team alignment, appropriate resourcing, and consistent application of company policies across the field engagement team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development of team training, onboarding, and engagement playbooks for Clinical Engagement Leads in collaboration with Clinical Operations and Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee team contributions to IIS (investigator-initiated study) identification and evaluation — ensuring scientifically relevant IIS concepts are appropriately flagged, reviewed, and tracked in coordination with Medical Affairs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee data quality and compliance of investigator interactions, site assessments, and clinical engagement activities recorded by the team in the CRM system, in accordance with company policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelor’s degree in scientific or related discipline. Advanced degree preferred — MS or MPH in a relevant clinical, biomedical, or pharmaceutical sciences discipline.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;7+ years of experience in clinical operations, clinical development, clinical research, or a field-based clinical engagement role within the pharmaceutical or biotech industry,\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of direct people management experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading, coaching, and developing field-based or matrixed teams, in addition to managing investigator relationships and supporting clinical trial site activation and enrollment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience collaborating with CROs, investigative sites, field medical teams, and HR/talent partners, including MSL partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific and clinical knowledge of immunology and inflammation — including disease biology, standard of care, clinical trial design considerations, and the competitive clinical research landscape across relevant I\u0026amp;amp;I indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in clinical trial site management and investigator engagement strategy including site feasibility assessment, investigator identification and qualification, site initiation support, and enrollment optimization with the ability to set direction and review team-level recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with clinical operations tools including CTMS, CRM platforms (e.g., Veeva), and site management systems; experience overseeing team documentation of field activities to GCP and compliance standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced people leader who manages and develops a team of field-based professionals independently, prioritizes team objectives strategically, and operates with minimal supervision across a broad geography.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coaching-oriented leader who builds genuine, long-term relationships with team members based on trust, accountability, and authentic commitment to their professional growth and to supporting research excellence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive performance manager who consistently translates team and field observations into actionable insights and coaching that improve program strategy, site selection, and enrollment performance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional interpersonal and coaching communication skills — engages team members in substantive performance and development conversations, and can credibly discuss Beeline’s pipeline, protocol design, and I\u0026amp;amp;I disease areas with investigators when needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear and structured internal communicator — provides concise, actionable team performance and field intelligence updates to Clinical Operations, Clinical Development and Medical Affairs leadership through regular written and verbal reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Credible external ambassador — represents Beeline’s science and organizational values at investigator meetings, scientific conferences, and site visits with professionalism, authority, and genuine enthusiasm for the organization’s mission.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at navigating complex stakeholder environments — communicates effectively with team members, academic physicians, research coordinators, site administrators, and IRB contacts across diverse clinical research settings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 70%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary 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;£130,000 GBP\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035447009,"name":"Clinical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4054775009,"name":"United Kingdom","location":"United Kingdom","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4434595009","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":4253967009,"location":{"name":"Durham, North Carolina, United States"},"metadata":null,"id":4434595009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"150","title":"Director, CMC Product Development - Small Molecule","company_name":"Beeline Medicines","first_published":"2026-10-05T21:30:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, CMC Product Development – Small Molecule is a senior technical and operational leader responsible for\u0026amp;nbsp;the end-to-end CMC development of small molecule drug product candidates, from early formulation through process development, clinical supplies, and regulatory submission. Reporting to the Executive Director, CMC Product Development, this individual drives the drug product development activities on assigned programs. This role carries no direct reports but works cross-functionally with internal teams and external CDMO drug product partners. It requires deep expertise in small molecule formulation science and manufacturing, experience in taking programs through late-stage development and filing, and ability to make sound technical decisions \u0026amp;nbsp;in a pre-commercial biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as\u0026amp;nbsp;\u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define and execute drug product development strategy for assigned small molecule programs, including formulation approach, manufacturing platform, and the development roadmap required to support the clinical and regulatory plan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead formulation development activities for small molecule drug candidates across all clinical phases, including excipient screening, compatibility studies, formulation optimization, and selection of final drug product composition for clinical and commercial manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct and oversee drug product process development, technical transfer, scale-up, process optimization, registration batch execution, and process validation / PPQ for solid oral dosage forms (tablets, capsules) and other small molecule drug delivery systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary technical interface with CDMO drug product teams for assigned programs, defining the scope of activities, providing scientific oversight of formulation and manufacturing campaigns, document review, and deviation resolution. Hold partners accountable to quality and timeline commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review drug product sections of regulatory submissions (IND, IMPD, NDA, MAA) including formulation descriptions, manufacturing process narratives, container-closure justifications, control strategies and process validation approaches. Lead the technical response to FDA and EMA questions on drug product topics and support health authority meetings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Integrate Quality by Design (QbD) principles and Design of Experiments (DoE) into formulation and process development decisions, establishing critical quality attributes (CQAs), critical process parameters (CPPs), and design spaces.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaboration with Analytical Development to define drug product release and stability specification, in-process controls, and comparability strategies for formulation and process changes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead packaging development and container-closure system selection for clinical and commercial drug product presentations, including compatibility assessment,\u0026amp;nbsp; and child-resistant packaging requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to clinical supply planning by providing manufacturing timelines, batch size projections, and drug product release schedules to the Clinical Supply Chain function in support of trial startup, enrollment milestones and uninterrupted clinical supply.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate drug delivery technology options and novel dosage form strategies for pipeline candidates, providing formulation feasibility assessments and manufacturability input during candidate selection and early development planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to CMC due diligence assessments and portfolio planning by evaluating the manufacturability and development feasibility of small molecule drug product candidates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, or a closely related discipline preferred, or equivalent industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of pharmaceutical drug product development and manufacturing experience focused on small molecules in pharmaceutical or biotechnology industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of serving as the primary scientific lead on formulation and drug product process development programs from early to late clinical phases.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep technical expertise in solid oral dosage form development (immediate release, modified release, amorphous solid dispersions), including formulation selection, manufacturing process development, scale up, technical transfer, commercial process optimization, and validation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in selecting and managing external partner relationships (CDMOs and contract laboratories), including technical oversight, work order management, change control, deviation resolution, and performance monitoring.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of ICH Q8/Q9/Q10/Q11, cGMP requirements and FDA/EMA drug product development expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience authoring drug product sections of INDs, IMPDs, and NDA filings and contributing to FDA or EMA responses on formulation, manufacturing, and drug product control strategy topics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of operating effectively in a pre-commercial, resource-constrained environment — balancing strategic vision with hands-on execution and infrastructure building.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing cross-functional stakeholder relationships at the senior level, with the ability to influence without authority and align diverse teams around shared program goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills, with a track record of authoring high-quality regulatory documents, scientific reports, and executive-level presentations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective collaborator with a track record of building productive working relationships across CMC functions, Clinical Development, Clinical Pharmacology, Regulatory Affairs, and Quality in a team-oriented environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organized and detail-oriented communicator who can manage competing priorities, proactively flag risks, and keep cross-functional stakeholders aligned on timelines and deliverable status.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 20%+ as needed of time or more including occasional overnight stay driven by business need.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$199,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$258,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035448009,"name":"CMC","child_ids":[],"parent_id":null}],"offices":[{"id":4038675009,"name":"Durham, NC Office","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4407708009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4235913009,"location":{"name":"United States"},"metadata":null,"id":4407708009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"138","title":"Director, Medical Writing","company_name":"Beeline Medicines","first_published":"2026-09-15T18:14:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, Medical Writing is a hands-on leadership role responsible for clear scientific messaging and for the development, coordination, and delivery of high-quality regulatory, nonclinical, clinical, and other scientific documents in support of the company\u0026#39;s I\u0026amp;amp;I pipeline. This position combines active document authorship with functional leadership of medical writing, ensuring that deliverables meet high standards of scientific accuracy, regulatory compliance, and clarity.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director owns the design and implementation of medical writing processes, templates, and standards, builds and manages internal writing capability, and directs the selection, oversight, and performance of external writing vendors within an agreed budget. The role partners closely with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, and external vendors to plan, author, review, and deliver documents supporting critical regulatory milestones, including INDs, amendments, briefing packages, and selected NDA/BLA components.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is expected to remain closely involved in the hands-on execution of core documents while carrying accountability for people management, vendor and budget management, and delivery across multiple concurrent programs as submission activity expands.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Remote - \u0026lt;/strong\u0026gt;This position is designated as remote; the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company\u0026#39;s discretion based on business need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own day to day execution of medical writing activities, authoring, coordinating, and reviewing key clinical and regulatory documents, including protocols and amendments, CSRs, IBs, SAPs, ICFs, INDs/CTAs, and selected BLA/NDA components, ensuring scientific accuracy, regulatory compliance, and consistency of content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to defining the strategy for submission narratives and key messages, leading scientific messaging consistency across CTD modules. Represent Medical Writing in cross functional and governance forums and drive alignment on submission strategy and document readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct planning and sequencing of document deliverables with Clinical Development, Nonclinical, Biostatistics, Safety, and Regulatory Affairs; own integrated timelines and trackers across concurrent programs, coordinate cross functional review cycles, anticipate and mitigate bottlenecks, and provide regular, transparent status updates to cross functional teams and leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and develop medical writing staff and contract writers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage medical writing vendors, including selection, scope definition, deliverable tracking, quality oversight, and performance review. Own the Medical Writing budget and forecast internal FTE and vendor capacity against the program plan.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish, document, and maintain the process for authoring, review, QC, and approval of regulatory documents submitted to health authorities, including SOPs, style guides, and templates aligned with ICH and regional requirements. Develop and deliver training to the cross functional team to ensure adoption of the agreed process.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support Health Authority briefing documents, meeting request packages, and written responses to Agency queries.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage the Medical Writing function budget and resource planning, including FTE capacity and vendor utilization forecasting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree (PhD, PharmD, or master\u0026#39;s level) in life sciences, pharmacology, biomedical sciences, or a related discipline required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 10+ years of medical writing experience in the pharmaceutical or biotech industry,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience authoring and overseeing regulatory submissions in ICH CTD format, including CSRs, ISS/ISE, IBs, and IND/CTA packages.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep scientific expertise in immunology, inflammation, or autoimmune disease is preferred, with the ability to rapidly acquire technical knowledge in new therapeutic areas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple concurrent document deliverables and writing teams in a high-priority regulatory environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge of FDA and EMA regulatory writing requirements, ICH E3, E6, E8, and M4 guidelines, and applicable pharmacovigilance documentation standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience developing and enforcing Medical Writing SOPs, style guides, and document templates in a regulated pharmaceutical environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with document management systems, electronic submission tools, and publishing platforms such as Veeva Vault or equivalent.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong publication planning experience, including familiarity with ICMJE authorship guidelines, journal submission processes, and scientific congress submission requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with AI-assisted authoring and review tools applied to regulatory and clinical documents is strongly preferred, including practical understanding best prompt practices, limitations, quality control requirements, and appropriate use in a regulated environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building or scaling a Medical Writing function in an early-stage or rapidly growing biotech organization is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead, mentor, and develop cross-functional teams in a fast-paced, resource-constrained biotech or pharmaceutical environment; fosters a culture of accountability, inclusion, and continuous learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of influencing without authority across organizational boundaries, driving alignment among senior stakeholders, and building consensus on complex scientific or operational priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional written and verbal communication skills with demonstrated ability to translate complex scientific, regulatory, or operational content for diverse audiences, including executive leadership, clinical teams, and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at preparing and delivering compelling presentations, briefing documents, and strategic updates to cross-functional leadership teams and board-level stakeholders.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$199,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$258,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035451009,"name":"Regulatory \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036151009,"name":"Remote (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4473598009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4289096009,"location":{"name":"United States"},"metadata":null,"id":4473598009,"updated_at":"2026-10-29T20:06:42-04:00","requisition_id":"159","title":"Global Pharmacovigilance Medical Director","company_name":"Beeline Medicines","first_published":"2026-10-29T20:06:42-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Pharmacovigilance Medical Director is the senior medical authority within the company\u0026#39;s drug safety function, responsible for providing expert medical and scientific leadership across all pharmacovigilance activities supporting the immunology and inflammation (I\u0026amp;amp;I) pipeline, including the company\u0026#39;s lead lupus program. This role serves as the primary physician voice for benefit-risk evaluation, signal assessment, and safety governance, ensuring that patient safety is upheld as the foundational principle of all clinical development and post-market activities. The Medical Director partners closely with the Head of Pharmacovigilance, Clinical Development, Regulatory Affairs, Medical Affairs, and external Health Authorities to provide medically sound, strategically aligned safety leadership at a critical stage of the company\u0026#39;s growth.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Remote -\u0026amp;nbsp;\u0026lt;/strong\u0026gt;This position is designated as remote; the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company\u0026#39;s discretion based on business need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior medical expert and physician for safety science and pharmacovigilance activities, providing authoritative medical judgment on individual case safety reports (ICSRs), aggregate safety analyses, signal evaluations, and benefit-risk assessments across the I\u0026amp;amp;I portfolio.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the medical review and clinical data interpretation of safety data arising from clinical trials, spontaneous reports, literature, and real-world sources, ensuring timely, accurate, and scientifically rigorous assessment of all pharmacovigilance data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct the development and continuous maintenance of the company\u0026#39;s benefit-risk framework, providing medical leadership in benefit-risk evaluations for regulatory submissions, label updates, and Health Authority safety communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the discussion at the company\u0026#39;s Safety surveillance governance, providing medical and strategic direction on safety signal management, escalation procedures, and corrective action planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the medical content and scientific quality of all aggregate safety reports, and regulatory submission dossiers for safety content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Development on the medical oversight of Data Safety Monitoring Board (DSMB) activities, clinical trial safety monitoring plans, safety risk mitigation plans (e.g.stopping rules), and protocol-level safety sections for all active and planned studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide expert medical input to Risk management plans and relevant regulatory documents through developmental cycle of the programs, and risk minimization measure design, execution, and effectiveness assessment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical leadership and scientific mentorship to the Pharmacovigilance team, including PV Scientists, and other functions (e.g. Medical Writers, and Operations personnel) establishing a culture of medical excellence and patient-first decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Medical degree (MD or DO) required; board certification or eligibility in immunology, rheumatology, internal medicine, or a relevant specialty experience in autoimmune disease is strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of combined clinical and pharmaceutical/biotech industry experience, with at least 2-3 years of dedicated pharmacovigilance or drug safety experience preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise serving as a physician-of-record for pharmacovigilance programs, including ICSR medical review, signal evaluation, benefit-risk assessment, and aggregate safety reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of global safety and pharmacovigilance regulations including FDA guidance, EU GVP Modules I–XVI and ICH guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience providing medical leadership for safety surveillance plan, and benefit-risk assessment, and submissions for IND and NDA/BLA, as well as direct authorship or oversight of complex safety narratives for regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience engaging with global Health Authorities on pharmacovigilance topics, including regulatory meeting preparation, written responses to safety queries, and inspection support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead or participate in DSMB oversight, clinical trial safety monitoring, and safety governance committee activities at the sponsor level.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience contributing to Risk Management Plans (RMPs) and REMS programs, including development of risk minimization measures and assessment of effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead, mentor, and develop cross-functional teams in a fast-paced, resource-constrained biotech or pharmaceutical environment; fosters a culture of accountability, inclusion, and continuous learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of influencing without authority across organizational boundaries, driving alignment among senior stakeholders, and building consensus on complex scientific or operational priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional written and verbal communication skills with demonstrated ability to translate complex scientific, regulatory, or operational content for diverse audiences, including executive leadership, clinical teams, and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at preparing and delivering compelling presentations, briefing documents and regulatory responses, and strategic updates to cross-functional leadership teams and board-level stakeholders.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$266,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$344,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035452009,"name":"Pharmacovigilance","child_ids":[],"parent_id":null}],"offices":[{"id":4036151009,"name":"Remote (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4458173009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4279077009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4458173009,"updated_at":"2026-10-19T15:27:26-04:00","requisition_id":"156","title":"IT Support Analyst","company_name":"Beeline Medicines","first_published":"2026-10-19T15:27:26-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The IT Support Analyst is an on-site technology resource for the assigned office, delivering reliable day-to-day desktop and end user support and assisting with executive technology, conference room systems, and live event production. Reporting to the Senior Manager, IT End User Services, this role troubleshoots hardware, software, network, and M365 issues for office-based employees while working alongside senior team members to support executive-facing meetings and events. This is a fully on-site, hands-on role for a developing IT professional with strong customer service skills, solid technical fundamentals, and the composure to support high-visibility events with guidance from senior staff.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Onsite - \u0026lt;/strong\u0026gt;This position is fully on-site and requires the incumbent to work from Beeline Medicines\u0026#39; office on a full-time basis (Monday through Friday). Regular, in-person attendance is an essential function of this role.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Desktop and End User Support: Provide first-level and select second-level IT support for office-based employees, including troubleshooting and configuring hardware, software, network connectivity, printing, and M365 application issues. Resolve tickets within established SLAs, escalate issues that exceed scope to the Senior IT Support Analyst, Senior Manager, or MSP service desk, and document all support activity in the ITSM ticketing system.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executive Technology Support: Assist the Senior IT Support Analyst in providing priority support to C-suite executives and visiting board members, including workstation setup, device configuration, and pre-meeting technology checks. Serve as backup on-site technology contact for executive requests as directed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Event Technology and AV Support: Assist with setup, operation, and breakdown of AV equipment for board presentations, analyst meetings, investor events, and company town halls. Participate in rehearsals, monitor live feeds, and troubleshoot common issues in real time under the direction of senior team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conference Room and Office Technology: Perform routine checks and preventive maintenance on conference room technology, including Teams Rooms systems, displays, cameras, microphones, and wireless presentation devices. Set up temporary meeting spaces and support guest Wi-Fi access, loaner devices, and visitor connectivity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Endpoint Deployment and Lifecycle Management: Image, configure, and deploy laptops, desktops, and peripherals using standard build processes. Coordinate hardware delivery to end users, maintain accurate inventory records for endpoints and loaner devices, and manage office hardware and supplies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identity and Access Management Support: Support account provisioning, password resets, MFA troubleshooting, group membership updates, and access requests following established procedures.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Bachelor\u0026#39;s degree in Information Technology, Computer Science, or related discipline, or equivalent years of industry experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3 years of hands-on IT support experience, including desktop support and end user troubleshooting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Microsoft 365 applications and basic administration, including account management; exposure to Entra ID and Intune preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with an ITSM ticketing system (ServiceNow, Jira Service Management, or equivalent).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to conference room systems, video conferencing, or live event/AV support preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Microsoft 365 applications: Outlook, Teams, OneDrive, SharePoint, with user-level troubleshooting and account management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of conference room technology and video conferencing, including Teams Rooms; AV and webcasting experience a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic networking: Wi-Fi troubleshooting, printer connectivity, VPN, and DNS resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in a life sciences, biotech, or pharmaceutical company is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional, service-oriented presence when working with executives, board members, and external guests.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Takes ownership of assigned tasks and seeks guidance appropriately from senior team members.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reliable follow-through: completes assigned work on time without needing reminders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear documentation habits: writes accurate ticket notes and follows established procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Schedule: Standard business hours, with occasional evening, weekend, or on-call availability required to support events, system maintenance, upgrades, or urgent issues outside normal hours.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements of Position:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical demands: Frequent use of a computer keyboard and monitor for extended periods; occasional lifting of computer equipment, monitors, or peripherals (up to 25–50 lbs); ability to bend, kneel, or reach to install or troubleshoot hardware under desks or in server racks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel: Minimal to occasional travel may be required between office locations or to support remote sites/end users as needed.\u0026amp;nbsp;\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$77,000\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;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035454009,"name":"Information Technology","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4439208009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4256635009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4439208009,"updated_at":"2026-10-08T15:59:51-04:00","requisition_id":"153","title":"Medical Director, Clinical Development","company_name":"Beeline Medicines","first_published":"2026-10-08T15:59:51-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Medical Director, Clinical Development – is a therapeutic and disease area specialist who will play a key role in advancing innovative therapies for patients with immunology diseases through high-quality design and execution of clinical trials. In this role, you will provide medical leadership across a range of clinical development activities, including but not limited to: \u0026amp;nbsp;study design, study execution, the monitoring of patient safety, data interpretation, and contribution to regulatory and scientific deliverables. As an internal scientific leader in the field, you will provide input into the overall clinical development strategy for the asset and incorporate insights from key opinion leader interactions into both study design and development strategy.\u0026amp;nbsp; This role involves working closely with internal cross-functional partners across a range of disciplines to drive high-quality clinical programs in a fast-paced biotech environment\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as\u0026amp;nbsp;\u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and provide medical oversight for assigned clinical trials including; protocol development, study conduct, medical monitoring, data review \u0026amp;amp; interpretation, and clinical study reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to clinical development strategy and program plans by integrating scientific rationale, regulatory requirements, safety considerations, operational feasibility, and business objectives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide medical leadership on trial design, including endpoint selection, eligibility criteria, dose rationale, biomarker strategy, risk-based monitoring, and interim analysis frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor real time data collection throughout study conduct ensuring robust study conduct and protocol adherence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support pharmacovigilance activities during trial conduct — monitor patient safety and benefit-risk throughout study conduct through review of adverse events, serious adverse events, laboratory data, safety narratives, and aggregate safety information, and contribute to related safety governance activities in coordination with the Global PV Medical Director\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key medical resource for investigative sites, external advisors, and clinical investigators, ensuring patients meet the appropriate eligibility criteria, responding to clinical and safety inquiries and supporting external interactions, advisory boards, and scientific communications as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and conduct peer-to-peer scientific exchange with KMEs, investigators, and HCPs — sharing clinical and emerging data, discussing unmet medical needs, and gathering external insights that inform overall development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review, author, and contribute to key clinical and regulatory documents, including protocols, protocol amendments, investigator brochures, informed consent forms, clinical study reports, briefing materials, and health authority responses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory interactions and submissions by providing medical and scientific input for agency meetings, annual reports, and clinical sections of regulatory filings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the clinical development lead for an asset if required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Advanced clinical degree (MD or DO) or MD/PhD required. Board certification or clinical training in rheumatology, nephrology, immunology, or a related specialty strongly preferred. Additional advanced degree (PhD, MPH, or MBA) is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of combined clinical and pharmaceutical/biotech industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience treating, or managing lupus (SLE and/or CLE)and/or systemic sclerosis patients/clinical programs strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep scientific expertise in autoimmune disease — rheumatology, specifically lupus (SLE and/or CLE) or systemic sclerosis, preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience of phase 1-3 clinical studies in particular; authoring clinical trial protocols, clinical development plans and regulatory submission documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep clinical and scientific expertise in immunology and inflammation— including command of disease mechanisms, clinical trial landscapes, standard of care evolution, regulatory developments, and emerging therapeutic approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to identify, characterize, and mitigate clinical, operational, and regulatory risks across multi-site, multinational clinical programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead and influence cross-functional teams in a matrixed, fast-paced biotech or pharmaceutical environment without direct line authority\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to build alignment across diverse internal and external stakeholders, including senior leadership, clinical operations, regulatory, and commercial partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track record of driving program-level decisions with clarity and accountability, balancing scientific rigor with business urgency in resource-constrained settings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional scientific communication skills, with the ability to articulate complex medical and clinical data to senior leadership, health authorities, clinical investigators, and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated scientific writing proficiency, including the ability to evaluate and present complex data sets in regulatory documents, clinical study reports, and scientific publications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at facilitating high-stakes discussions — including advisory boards, cross-functional program reviews, and health authority interactions — with confidence and precision\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$266,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$340,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035446009,"name":"Clinical Development","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4391998009","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":4227117009,"location":{"name":"China"},"metadata":null,"id":4391998009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"121","title":"Medical Science Liaison / Senior Medical Science Liaison - China","company_name":"Beeline Medicines","first_published":"2026-09-01T18:41:14-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking talented field-based scientific professionals to join our Medical Affairs team as a Medical Science Liaison (MSL) or Senior Medical Science Liaison (Senior MSL) within our Immunology \u0026amp;amp; Inflammation (I\u0026amp;amp;I) therapeutic area. Both roles are central to building scientific awareness and advocacy for Beeline\u0026#39;s pipeline, supporting investigator-initiated research, and facilitating meaningful peer-to-peer scientific exchange. The MSL level focuses on building foundational field excellence with progressive independence, while the Senior MSL operates with full strategic autonomy, leads senior KOL relationships, and contributes directly to Medical Affairs strategy and team development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;China and other APAC countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to development and refinement of medical strategy through field insights and HCP, KME, and investigator engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute territory plans aligned with organizational priorities and data milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage a defined territory of KME and HCP relationships within the I\u0026amp;amp;I therapeutic area — identifying, mapping, and engaging scientific thought leaders, clinical investigators, and academic centers relevant to Beeline\u0026#39;s pipeline under the direction of Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead segmentation (Tier 1/2/3) development, strategic engagement plans and longitudinal relationship ownership with HCPs, KMEs, and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct peer-to-peer scientific exchange with KMEs, HCPs, and clinical investigators — sharing clinical and preclinical data, presenting pipeline updates, and discussing unmet medical needs in I\u0026amp;amp;I in a balanced, compliant, and scientifically rigorous manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial awareness and site identification efforts by engaging with potential investigators and academic institutions, facilitating scientific discussions that may support site initiation and patient enrollment for organization’s I\u0026amp;amp;I programs. Serve as the key resource for scientific exchange as the ‘face of the sponsor’ with clinical site investigators from site start-up through end of study closeout in close collaboration with Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited medical information requests from HCPs, KMEs, and/or investigators in a timely, accurate, and compliant manner — in partnership with Medical Information and in accordance with applicable regulatory and compliance guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the field-based scientific resource for HCP, KME and investigator interactions related to investigator-initiated studies (IIS) — supporting the IIS process by facilitating scientific discussions and coordinating with internal Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support identification of evidence gaps and contribute to evidence generation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate, synthesize, and translate insights into strategic recommendations, with a focus on quality and actionability — including KME perspectives, competitive intelligence, clinical practice trends, and unmet need observations — back to Medical Affairs, Clinical Development, and other cross functional teams in a structured and timely manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at scientific conferences, medical congresses, and advisory board meetings within the I\u0026amp;amp;I therapeutic area — engaging with scientific thought leaders and gathering data that informs the organization\u0026#39;s medical and pipeline strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3 years of MSL or related field-based medical affairs experience in the pharmaceutical or biotech industry, with experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific and clinical knowledge of immunology and inflammation — demonstrates foundational understanding of disease mechanisms, treatment landscapes, and emerging therapeutic approaches and is actively building depth through ongoing learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret and communicate clinical and scientific data — including study design, statistical concepts, and benefit-risk assessment — in peer-to-peer HCP KME, and investigator settings, with continued development of sophistication over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working proficiency in CRM platforms (e.g., Veeva) for field activity documentation, HCP, KME, and investigator mapping, and territory management — developing consistent documentation habits that reflect compliance and organizational standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building knowledge of medical affairs compliance frameworks — including FDA and EMA regulations, PhRMA guidelines, and the distinctions between on-label and off-label scientific exchange — with active demonstration of compliant field behavior in all interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing field independence — operates with guidance from Medical Affairs leadership, demonstrates growing ability to manage territory priorities, plan engagement calendars, and execute field activities with increasing self-direction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team contributor and active learner — engages constructively in MSL team discussions, shares field observations openly, and demonstrates intellectual curiosity and a growth mindset in building scientific and professional capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific communication skills — able to present and discuss Beeline\u0026#39;s I\u0026amp;amp;I data clearly and accurately with HCPs, KMEs and investigators, with active development of the depth, nuance, and adaptability that characterizes expert-level scientific dialogue.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building active listening and field intelligence skills — demonstrates growing ability to capture insights and clinical practice observations accurately and translate them into concise, useful internal communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Growing confidence in varied engagement settings — developing effectiveness in one-on-one HCP/KME/investigator meetings, small group scientific discussions, and conference interactions, with continued development toward advisory board and large group facilitation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Senior Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and manage a strategically defined territory of senior KOL, clinical investigator, and academic center relationships — developing long-term, individualized engagement plans that align KOL scientific interests with organizations pipeline priorities and medical affairs objectives with full independence. Develop and continuously refine territory strategy based on evolving data milestones, KME influence mapping, and clinical development priorities; ensuring optimal allocation of time and resources to maximize impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct sophisticated, peer-to-peer scientific exchange with senior thought leaders, clinical investigators, and HCPs — including discussions of emerging clinical data, nuanced benefit-risk considerations, and evolving disease paradigms relevant to organization\u0026#39;s I\u0026amp;amp;I programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior field resource for clinical trial support — including investigator identification, scientific site engagement, and contributions to enrollment strategy discussions in close collaboration with Clinical Development and Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and manage investigator-initiated study (IIS) relationships within the territory — serving as the primary scientific point of contact for investigators, facilitating the IIS review process, and maintaining ongoing scientific engagement with funded IIS sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively synthesize and present strategic KOL engagement insights and field intelligence — delivering actionable recommendations to Medical Affairs leadership, Clinical Development, and other strategy teams that influence organizational decision-making. Demonstrate measurable impact on key Medical Affairs priorities, including KME engagement quality, contribution to clinical trial enrollment and site activation, and influence on strategic decision-making through actionable field insights.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of MSL scientific training materials, field tools, and disease area resources — applying territorial expertise and scientific depth to strengthen the broader MSL team\u0026#39;s capabilities and field effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at major national and international scientific conferences, advisory boards, and KOL forums within I\u0026amp;amp;I — serving as a senior scientific ambassador with the credibility and confidence to engage the field\u0026#39;s most influential voices. Play a leadership role in advisory board development and execution; including KME identification, scientific input into agenda design, and synthesis of outcomes into strategic recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of MSL or field-based medical affairs experience in the pharmaceutical or biotech industry, with demonstrated expertise in immunology, inflammation, or a closely related therapeutic area preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior involvement in IIS management or clinical trial support activities preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific and clinical expertise in immunology and inflammation — demonstrates deep, current knowledge of disease biology, treatment algorithms, clinical trial endpoints, emerging mechanisms, and the competitive I\u0026amp;amp;I landscape, applied with confidence in complex scientific discussions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert ability to interpret, contextualize, and communicate complex clinical and translational data — including study design nuances, subgroup analyses, and evolving safety/efficacy profiles — in substantive peer-level discussions with senior KOLs and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established proficiency in Veeva CRM and medical affairs field tools; experience with digital engagement platforms and virtual scientific exchange, with consistent documentation quality that reflects field excellence standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage AI-driven and omnichannel engagement strategies to complement in-person interactions; optimizing reach, frequency, and scientific exchange effectiveness with key stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep working knowledge of medical affairs compliance — including PhRMA guidelines, FDA regulations, and IIS management frameworks — demonstrated through a sustained record of compliant, high-quality field interactions and the ability to guide junior colleagues on compliance questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operates with full strategic independence — manages territory, KOL engagement plans, and field priorities without day-to-day guidance; proactively identifies opportunities and addresses challenges with sound judgment and organizational awareness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly sophisticated scientific communicator — engages senior KOLs, principal investigators, and academic thought leaders in nuanced, data-rich scientific dialogue that builds long-term credibility and trust for Beeline\u0026#39;s I\u0026amp;amp;I platform.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at synthesizing and presenting complex field intelligence in structured, executive-ready internal communications — delivers strategic actionable recommendations and tracking downstream impact to refine engagement strategy and maximize organizational value to Medical Affairs and clinical leadership with clarity and confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced facilitator and presenter — equally effective in one-on-one KOL settings, investigator meetings, advisory board participation, and large medical congress environments, with a demonstrated ability to adapt scientific communication style to audience needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4076257009,"name":"China","location":"China","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4392029009","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":4227137009,"location":{"name":"India"},"metadata":null,"id":4392029009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"122","title":"Medical Science Liaison / Senior Medical Science Liaison - India","company_name":"Beeline Medicines","first_published":"2026-09-01T19:12:15-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking talented field-based scientific professionals to join our Medical Affairs team as a Medical Science Liaison (MSL) or Senior Medical Science Liaison (Senior MSL) within our Immunology \u0026amp;amp; Inflammation (I\u0026amp;amp;I) therapeutic area. Both roles are central to building scientific awareness and advocacy for Beeline\u0026#39;s pipeline, supporting investigator-initiated research, and facilitating meaningful peer-to-peer scientific exchange. The MSL level focuses on building foundational field excellence with progressive independence, while the Senior MSL operates with full strategic autonomy, leads senior KOL relationships, and contributes directly to Medical Affairs strategy and team development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;India and other APAC countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to development and refinement of medical strategy through field insights and HCP, KME, and investigator engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute territory plans aligned with organizational priorities and data milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage a defined territory of KME and HCP relationships within the I\u0026amp;amp;I therapeutic area — identifying, mapping, and engaging scientific thought leaders, clinical investigators, and academic centers relevant to Beeline\u0026#39;s pipeline under the direction of Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead segmentation (Tier 1/2/3) development, strategic engagement plans and longitudinal relationship ownership with HCPs, KMEs, and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct peer-to-peer scientific exchange with KMEs, HCPs, and clinical investigators — sharing clinical and preclinical data, presenting pipeline updates, and discussing unmet medical needs in I\u0026amp;amp;I in a balanced, compliant, and scientifically rigorous manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial awareness and site identification efforts by engaging with potential investigators and academic institutions, facilitating scientific discussions that may support site initiation and patient enrollment for organization’s I\u0026amp;amp;I programs. Serve as the key resource for scientific exchange as the ‘face of the sponsor’ with clinical site investigators from site start-up through end of study closeout in close collaboration with Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited medical information requests from HCPs, KMEs, and/or investigators in a timely, accurate, and compliant manner — in partnership with Medical Information and in accordance with applicable regulatory and compliance guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the field-based scientific resource for HCP, KME and investigator interactions related to investigator-initiated studies (IIS) — supporting the IIS process by facilitating scientific discussions and coordinating with internal Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support identification of evidence gaps and contribute to evidence generation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate, synthesize, and translate insights into strategic recommendations, with a focus on quality and actionability — including KME perspectives, competitive intelligence, clinical practice trends, and unmet need observations — back to Medical Affairs, Clinical Development, and other cross functional teams in a structured and timely manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at scientific conferences, medical congresses, and advisory board meetings within the I\u0026amp;amp;I therapeutic area — engaging with scientific thought leaders and gathering data that informs the organization\u0026#39;s medical and pipeline strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3 years of MSL or related field-based medical affairs experience in the pharmaceutical or biotech industry, with experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific and clinical knowledge of immunology and inflammation — demonstrates foundational understanding of disease mechanisms, treatment landscapes, and emerging therapeutic approaches and is actively building depth through ongoing learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret and communicate clinical and scientific data — including study design, statistical concepts, and benefit-risk assessment — in peer-to-peer HCP KME, and investigator settings, with continued development of sophistication over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working proficiency in CRM platforms (e.g., Veeva) for field activity documentation, HCP, KME, and investigator mapping, and territory management — developing consistent documentation habits that reflect compliance and organizational standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building knowledge of medical affairs compliance frameworks — including FDA and EMA regulations, PhRMA guidelines, and the distinctions between on-label and off-label scientific exchange — with active demonstration of compliant field behavior in all interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing field independence — operates with guidance from Medical Affairs leadership, demonstrates growing ability to manage territory priorities, plan engagement calendars, and execute field activities with increasing self-direction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team contributor and active learner — engages constructively in MSL team discussions, shares field observations openly, and demonstrates intellectual curiosity and a growth mindset in building scientific and professional capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific communication skills — able to present and discuss Beeline\u0026#39;s I\u0026amp;amp;I data clearly and accurately with HCPs, KMEs and investigators, with active development of the depth, nuance, and adaptability that characterizes expert-level scientific dialogue.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building active listening and field intelligence skills — demonstrates growing ability to capture insights and clinical practice observations accurately and translate them into concise, useful internal communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Growing confidence in varied engagement settings — developing effectiveness in one-on-one HCP/KME/investigator meetings, small group scientific discussions, and conference interactions, with continued development toward advisory board and large group facilitation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Senior Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and manage a strategically defined territory of senior KOL, clinical investigator, and academic center relationships — developing long-term, individualized engagement plans that align KOL scientific interests with organizations pipeline priorities and medical affairs objectives with full independence. Develop and continuously refine territory strategy based on evolving data milestones, KME influence mapping, and clinical development priorities; ensuring optimal allocation of time and resources to maximize impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct sophisticated, peer-to-peer scientific exchange with senior thought leaders, clinical investigators, and HCPs — including discussions of emerging clinical data, nuanced benefit-risk considerations, and evolving disease paradigms relevant to organization\u0026#39;s I\u0026amp;amp;I programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior field resource for clinical trial support — including investigator identification, scientific site engagement, and contributions to enrollment strategy discussions in close collaboration with Clinical Development and Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and manage investigator-initiated study (IIS) relationships within the territory — serving as the primary scientific point of contact for investigators, facilitating the IIS review process, and maintaining ongoing scientific engagement with funded IIS sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively synthesize and present strategic KOL engagement insights and field intelligence — delivering actionable recommendations to Medical Affairs leadership, Clinical Development, and other strategy teams that influence organizational decision-making. Demonstrate measurable impact on key Medical Affairs priorities, including KME engagement quality, contribution to clinical trial enrollment and site activation, and influence on strategic decision-making through actionable field insights.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of MSL scientific training materials, field tools, and disease area resources — applying territorial expertise and scientific depth to strengthen the broader MSL team\u0026#39;s capabilities and field effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at major national and international scientific conferences, advisory boards, and KOL forums within I\u0026amp;amp;I — serving as a senior scientific ambassador with the credibility and confidence to engage the field\u0026#39;s most influential voices. Play a leadership role in advisory board development and execution; including KME identification, scientific input into agenda design, and synthesis of outcomes into strategic recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of MSL or field-based medical affairs experience in the pharmaceutical or biotech industry, with demonstrated expertise in immunology, inflammation, or a closely related therapeutic area preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior involvement in IIS management or clinical trial support activities preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific and clinical expertise in immunology and inflammation — demonstrates deep, current knowledge of disease biology, treatment algorithms, clinical trial endpoints, emerging mechanisms, and the competitive I\u0026amp;amp;I landscape, applied with confidence in complex scientific discussions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert ability to interpret, contextualize, and communicate complex clinical and translational data — including study design nuances, subgroup analyses, and evolving safety/efficacy profiles — in substantive peer-level discussions with senior KOLs and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established proficiency in Veeva CRM and medical affairs field tools; experience with digital engagement platforms and virtual scientific exchange, with consistent documentation quality that reflects field excellence standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage AI-driven and omnichannel engagement strategies to complement in-person interactions; optimizing reach, frequency, and scientific exchange effectiveness with key stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep working knowledge of medical affairs compliance — including PhRMA guidelines, FDA regulations, and IIS management frameworks — demonstrated through a sustained record of compliant, high-quality field interactions and the ability to guide junior colleagues on compliance questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operates with full strategic independence — manages territory, KOL engagement plans, and field priorities without day-to-day guidance; proactively identifies opportunities and addresses challenges with sound judgment and organizational awareness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly sophisticated scientific communicator — engages senior KOLs, principal investigators, and academic thought leaders in nuanced, data-rich scientific dialogue that builds long-term credibility and trust for Beeline\u0026#39;s I\u0026amp;amp;I platform.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at synthesizing and presenting complex field intelligence in structured, executive-ready internal communications — delivers strategic actionable recommendations and tracking downstream impact to refine engagement strategy and maximize organizational value to Medical Affairs and clinical leadership with clarity and confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced facilitator and presenter — equally effective in one-on-one KOL settings, investigator meetings, advisory board participation, and large medical congress environments, with a demonstrated ability to adapt scientific communication style to audience needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4076256009,"name":"India","location":"India","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4305465009","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":4179038009,"location":{"name":"Japan"},"metadata":null,"id":4305465009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"88","title":"Medical Science Liaison / Senior Medical Science Liaison - Japan","company_name":"Beeline Medicines","first_published":"2026-07-02T17:41:51-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking talented field-based scientific professionals to join our Medical Affairs team as a Medical Science Liaison (MSL) or Senior Medical Science Liaison (Senior MSL) within our Immunology \u0026amp;amp; Inflammation (I\u0026amp;amp;I) therapeutic area. Both roles are central to building scientific awareness and advocacy for Beeline\u0026#39;s pipeline, supporting investigator-initiated research, and facilitating meaningful peer-to-peer scientific exchange. The MSL level focuses on building foundational field excellence with progressive independence, while the Senior MSL operates with full strategic autonomy, leads senior KOL relationships, and contributes directly to Medical Affairs strategy and team development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Field-Based - \u0026lt;/strong\u0026gt;This position is field-based, and the incumbent will be expected to work within their assigned territory or region on behalf of the company. Regular travel within the designated geography is an inherent requirement of this role. Additional travel outside of the assigned territory may be required based on business need, including attendance at company meetings, training, or other organizational events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Territory Assignment Notice:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Japan and other APAC countries as assigned.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Notice: The geographic territory outlined for this position reflects current business needs and is subject to change at the discretion of the organization. Territory boundaries, state assignments, and regional alignments may be modified at any time based on evolving business priorities, organizational restructuring, or strategic initiatives. The selected candidate will be expected to adapt to any such changes as a condition of employment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Contribute to development and refinement of medical strategy through field insights and HCP, KME, and investigator engagement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute territory plans aligned with organizational priorities and data milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and manage a defined territory of KME and HCP relationships within the I\u0026amp;amp;I therapeutic area — identifying, mapping, and engaging scientific thought leaders, clinical investigators, and academic centers relevant to Beeline\u0026#39;s pipeline under the direction of Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead segmentation (Tier 1/2/3) development, strategic engagement plans and longitudinal relationship ownership with HCPs, KMEs, and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct peer-to-peer scientific exchange with KMEs, HCPs, and clinical investigators — sharing clinical and preclinical data, presenting pipeline updates, and discussing unmet medical needs in I\u0026amp;amp;I in a balanced, compliant, and scientifically rigorous manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial awareness and site identification efforts by engaging with potential investigators and academic institutions, facilitating scientific discussions that may support site initiation and patient enrollment for organization’s I\u0026amp;amp;I programs. Serve as the key resource for scientific exchange as the ‘face of the sponsor’ with clinical site investigators from site start-up through end of study closeout in close collaboration with Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Respond to unsolicited medical information requests from HCPs, KMEs, and/or investigators in a timely, accurate, and compliant manner — in partnership with Medical Information and in accordance with applicable regulatory and compliance guidelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the field-based scientific resource for HCP, KME and investigator interactions related to investigator-initiated studies (IIS) — supporting the IIS process by facilitating scientific discussions and coordinating with internal Medical Affairs leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support identification of evidence gaps and contribute to evidence generation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate, synthesize, and translate insights into strategic recommendations, with a focus on quality and actionability — including KME perspectives, competitive intelligence, clinical practice trends, and unmet need observations — back to Medical Affairs, Clinical Development, and other cross functional teams in a structured and timely manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at scientific conferences, medical congresses, and advisory board meetings within the I\u0026amp;amp;I therapeutic area — engaging with scientific thought leaders and gathering data that informs the organization\u0026#39;s medical and pipeline strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 3 years of MSL or related field-based medical affairs experience in the pharmaceutical or biotech industry, with experience in immunology, inflammation, or a related therapeutic area strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific and clinical knowledge of immunology and inflammation — demonstrates foundational understanding of disease mechanisms, treatment landscapes, and emerging therapeutic approaches and is actively building depth through ongoing learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to interpret and communicate clinical and scientific data — including study design, statistical concepts, and benefit-risk assessment — in peer-to-peer HCP KME, and investigator settings, with continued development of sophistication over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working proficiency in CRM platforms (e.g., Veeva) for field activity documentation, HCP, KME, and investigator mapping, and territory management — developing consistent documentation habits that reflect compliance and organizational standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building knowledge of medical affairs compliance frameworks — including FDA and EMA regulations, PhRMA guidelines, and the distinctions between on-label and off-label scientific exchange — with active demonstration of compliant field behavior in all interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing field independence — operates with guidance from Medical Affairs leadership, demonstrates growing ability to manage territory priorities, plan engagement calendars, and execute field activities with increasing self-direction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team contributor and active learner — engages constructively in MSL team discussions, shares field observations openly, and demonstrates intellectual curiosity and a growth mindset in building scientific and professional capabilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Developing scientific communication skills — able to present and discuss Beeline\u0026#39;s I\u0026amp;amp;I data clearly and accurately with HCPs, KMEs and investigators, with active development of the depth, nuance, and adaptability that characterizes expert-level scientific dialogue.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Building active listening and field intelligence skills — demonstrates growing ability to capture insights and clinical practice observations accurately and translate them into concise, useful internal communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Growing confidence in varied engagement settings — developing effectiveness in one-on-one HCP/KME/investigator meetings, small group scientific discussions, and conference interactions, with continued development toward advisory board and large group facilitation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Senior Medical Science Liaison Essential Duties and Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead and manage a strategically defined territory of senior KOL, clinical investigator, and academic center relationships — developing long-term, individualized engagement plans that align KOL scientific interests with organizations pipeline priorities and medical affairs objectives with full independence. Develop and continuously refine territory strategy based on evolving data milestones, KME influence mapping, and clinical development priorities; ensuring optimal allocation of time and resources to maximize impact.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct sophisticated, peer-to-peer scientific exchange with senior thought leaders, clinical investigators, and HCPs — including discussions of emerging clinical data, nuanced benefit-risk considerations, and evolving disease paradigms relevant to organization\u0026#39;s I\u0026amp;amp;I programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior field resource for clinical trial support — including investigator identification, scientific site engagement, and contributions to enrollment strategy discussions in close collaboration with Clinical Development and Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own and manage investigator-initiated study (IIS) relationships within the territory — serving as the primary scientific point of contact for investigators, facilitating the IIS review process, and maintaining ongoing scientific engagement with funded IIS sites.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively synthesize and present strategic KOL engagement insights and field intelligence — delivering actionable recommendations to Medical Affairs leadership, Clinical Development, and other strategy teams that influence organizational decision-making. Demonstrate measurable impact on key Medical Affairs priorities, including KME engagement quality, contribution to clinical trial enrollment and site activation, and influence on strategic decision-making through actionable field insights.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development of MSL scientific training materials, field tools, and disease area resources — applying territorial expertise and scientific depth to strengthen the broader MSL team\u0026#39;s capabilities and field effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Beeline at major national and international scientific conferences, advisory boards, and KOL forums within I\u0026amp;amp;I — serving as a senior scientific ambassador with the credibility and confidence to engage the field\u0026#39;s most influential voices. Play a leadership role in advisory board development and execution; including KME identification, scientific input into agenda design, and synthesis of outcomes into strategic recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field. Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years of MSL or field-based medical affairs experience in the pharmaceutical or biotech industry, with demonstrated expertise in immunology, inflammation, or a closely related therapeutic area preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior involvement in IIS management or clinical trial support activities preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical-stage biotech experience a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced scientific and clinical expertise in immunology and inflammation — demonstrates deep, current knowledge of disease biology, treatment algorithms, clinical trial endpoints, emerging mechanisms, and the competitive I\u0026amp;amp;I landscape, applied with confidence in complex scientific discussions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expert ability to interpret, contextualize, and communicate complex clinical and translational data — including study design nuances, subgroup analyses, and evolving safety/efficacy profiles — in substantive peer-level discussions with senior KOLs and investigators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established proficiency in Veeva CRM and medical affairs field tools; experience with digital engagement platforms and virtual scientific exchange, with consistent documentation quality that reflects field excellence standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Leverage AI-driven and omnichannel engagement strategies to complement in-person interactions; optimizing reach, frequency, and scientific exchange effectiveness with key stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep working knowledge of medical affairs compliance — including PhRMA guidelines, FDA regulations, and IIS management frameworks — demonstrated through a sustained record of compliant, high-quality field interactions and the ability to guide junior colleagues on compliance questions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operates with full strategic independence — manages territory, KOL engagement plans, and field priorities without day-to-day guidance; proactively identifies opportunities and addresses challenges with sound judgment and organizational awareness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly sophisticated scientific communicator — engages senior KOLs, principal investigators, and academic thought leaders in nuanced, data-rich scientific dialogue that builds long-term credibility and trust for Beeline\u0026#39;s I\u0026amp;amp;I platform.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at synthesizing and presenting complex field intelligence in structured, executive-ready internal communications — delivers strategic actionable recommendations and tracking downstream impact to refine engagement strategy and maximize organizational value to Medical Affairs and clinical leadership with clarity and confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced facilitator and presenter — equally effective in one-on-one KOL settings, investigator meetings, advisory board participation, and large medical congress environments, with a demonstrated ability to adapt scientific communication style to audience needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Professional fluency in English (written and verbal) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to safely and successfully operate a motor vehicle is required. Valid Driver’s License and a driving record in compliance with company standards\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 50%+ as needed of time or more including occasional overnight stay driven by business need.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to work evenings and weekends, as needed, for physician or patient events (both in person and virtual).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Depending on geography, must have the ability to manage a multi-state territory with diverse customer base.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4036152009,"name":"Field Based (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4402940009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4233115009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4402940009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"133","title":"Senior Director, Clinical Pharmacology","company_name":"Beeline Medicines","first_published":"2026-09-10T19:00:40-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Clinical Pharmacology provides clinical pharmacology leadership across development programs, directing PK/PD strategy, modeling and simulation, and dose-selection activities to inform clinical trial design and regulatory submissions. Leads population PK, exposure-response, and other quantitative modeling efforts performed internally or through modeling vendors and translates the resulting insights into dose-selection rationale that shapes protocol design. Serves as the clinical pharmacology voice on cross-functional program teams and represents the function directly with health authorities during meetings and submission reviews. This role requires both technical modeling expertise and the credibility to defend clinical pharmacology strategy in high-stakes regulatory interactions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead clinical pharmacology strategy for assigned programs, including PK/PD study design and dose-selection rationale.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct population PK, exposure-response, and modeling and simulation analyses performed internally or by vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and review clinical pharmacology sections of INDs, NDAs/BLAs, and health authority responses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as clinical pharmacology lead on cross-functional program teams, advising on drug-drug interaction and special population studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent clinical pharmacology in interactions with health authorities (e.g., FDA/CHMP meetings), including authorship of relevant sections of briefing documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clinical pharmacology assessments to due diligence and licensing evaluations, as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee clinical pharmacology CRO and modeling vendor relationships and deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;PharmD, PhD in Clinical Pharmacology, Pharmacokinetics, Pharmacometrics, pharmaceutical sicences, or related discipline required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of clinical pharmacology experience in pharma/biotech, including leadership of PK/PD strategy across development-stage programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years of vendor management oversight experience with ability to manage and hold CRO/modeling vendors accountable for deliverable quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in immunology, inflammation, autoimmune disease, immune-mediated diseases, T-cell biology, cell therapy, biologics, gene therapy, or other novel therapeutic modalities preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in population PK/PD modeling, , and relevant software (e.g., NONMEM, R).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of ICH and FDA/EMA clinical pharmacology guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of drug-drug interaction and special population study design.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead clinical pharmacology strategy discussions with senior internal and external stakeholders, including regulators.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent scientific writing and presentation skills for regulatory submissions and health authority interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at defending clinical pharmacology strategy directly with health authorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage external CROs/vendors and coordinate study execution across multiple stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong project/program management capability, including timeline planning, cross-functional coordination, risk tracking, deliverable management, and issue escalation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate scientific and operational issues clearly to cross-functional teams and senior stakeholders.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$266,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$344,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4071531009,"name":"Clinical Pharmacology","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4373062009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4215618009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4373062009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"107","title":"Senior Director, GCP Quality Assurance","company_name":"Beeline Medicines","first_published":"2026-08-17T20:44:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, GCP Quality Assurance provides strategic leadership and operational oversight for Good Clinical Practice (GCP) Quality Assurance activities supporting the company’s clinical development programs. This role is accountable for ensuring that clinical trials are conducted, documented, and reported in compliance with applicable regulatory requirements, company policies, and global GCP standards while maintaining a continuous state of inspection readiness.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director serves as a senior QA leader and strategic partner to Clinical Operations, Regulatory Affairs, Pharmacovigilance, Data Management, Biostatistics, and external service providers. The role is accountable for GCP quality systems, clinical quality risk management, CRO and vendor oversight, audit strategy, inspection readiness, quality metrics, and the maturation of fit-for-purpose GCP processes that embed quality by design across the clinical lifecycle.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Define, implement, and continuously mature the GCP QA strategy aligned with clinical development objectives, corporate priorities, and global regulatory expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior GCP QA partner to Clinical Operations and cross-functional stakeholders, providing strategic guidance on GCP compliance, clinical quality risk management, and inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Champion a proactive culture of quality, compliance, patient safety, data integrity, and continuous improvement across clinical programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, lead, mentor, and develop GCP QA capability and/or external QA resources as the function scales.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure GCP processes are phase-appropriate, risk-based, compliant, scalable, and suitable for outsourced or hybrid clinical development models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead or provide senior QA oversight for the development, review, approval, implementation, and lifecycle management of GCP-related SOPs, policies, work instructions, and training materials.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide senior QA oversight for GCP activities conducted internally and by CROs, investigator sites, vendors, and other service providers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as sponsor QA counterpart to CRO QA groups and other external partner quality functions, ensuring clear standards, escalation pathways, and issue resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead GCP vendor qualification, risk-based audit strategy, issue escalation, performance oversight, and ongoing vendor governance using risk-based principles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review, approve, and maintain QA oversight of GCP-related quality agreements, vendor oversight plans, audit plans, and CAPA commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide senior QA review of key clinical and regulatory documents, as appropriate, to support clinical development quality and submission readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own the risk-based GCP audit program, including CRO audits, investigator site audits, vendor audits, TMF/eTMF audits, and system or process audits as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead GCP inspection readiness, inspection conduct, response development, commitment tracking, and follow-up; serve as a primary QA contact during health authority inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate inspection preparation activities, mock inspections, inspection logistics, response development, CAPA planning, and verification of regulatory observation closure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify, assess, escalate, and proactively mitigate GCP compliance risks, including protocol deviation trends, vendor performance concerns, audit findings, and inspection readiness gaps.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelor’s degree in a scientific or related discipline; advanced degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years of progressive GCP Quality Assurance or Clinical Quality experience within a biotech, pharmaceutical, or CRO environment, including significant leadership experience at the Director level or equivalent.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 3 years of people management preferred.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of global GCP requirements and clinical trial oversight expectations, including ICH E6, FDA regulations, EU Clinical Trials Regulation considerations, and inspection readiness expectations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with eTMF, clinical quality systems, and electronic GxP systems; familiarity with 21 CFR Part 11, data integrity principles, and Veeva or similar platforms preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading or managing GCP audits and regulatory inspections, including inspection preparation, conduct, response development, CAPA oversight, and follow-up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience overseeing CROs, clinical vendors, investigator sites, and other GCP service providers in outsourced or hybrid development models.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting late-stage, pivotal, or registrational clinical trials and related inspection readiness activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in risk-based quality management, ICH E6(R3) risk-proportionate approaches, quality metrics, and inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building, scaling, or maturing GCP QA capabilities in lean, virtual, or growing biotechnology organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Executive presence and strong cross-functional influence\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to balance compliance, patient safety, data integrity, and operational execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 20%+ as needed of time or more including occasional overnight stay driven by business need.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$266,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$344,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035451009,"name":"Regulatory \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4329272009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4193247009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4329272009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"97","title":"Senior Director, Regulatory Affairs CMC – Biologics","company_name":"Beeline Medicines","first_published":"2026-07-22T22:30:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Regulatory Affairs CMC – Biologics provides senior-level scientific and strategic regulatory leadership for all Chemistry, Manufacturing, and Controls (CMC) activities related to the company\u0026#39;s biologics assets within the immunology and inflammation (I\u0026amp;amp;I) portfolio, including monoclonal antibodies and other large molecule therapeutic modalities. This role is responsible for developing and executing biologics CMC regulatory strategies from early clinical development through BLA filing and post-approval lifecycle management, serving as the company\u0026#39;s foremost authority on biologics CMC regulatory science. The Senior Director collaborates closely with Process Development, Analytical Sciences, Quality, and external biologics CMOs to ensure that programs are developed, characterized, and submitted in alignment with FDA, EMA, and global Health Authority expectations for biological products. As a senior leader within the Regulatory Affairs organization, this individual also contributes to cross-functional regulatory strategy and plays a foundational role in shaping the company\u0026#39;s biologics CMC regulatory infrastructure.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead the CMC regulatory strategy for all biologics assets in the I\u0026amp;amp;I portfolio, from IND/CTA through BLA and MAA filing, including post-approval lifecycle management and labeling strategy for drug substance and drug product.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, review, and oversee the preparation of biologics CMC sections of global regulatory submissions in ICH CTD format, including INDs/CTAs, BLAs, MAAs, supplements, and post-approval variations, with accountability for scientific quality, completeness, and regulatory defensibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the company\u0026#39;s primary regulatory authority and strategic partner for biologics Process Development, Upstream and Downstream Manufacturing Sciences, Analytical Development, Formulation, and Quality functions on all CMC regulatory matters.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead Health Authority interactions related to biologics CMC topics, including FDA Type B and Type C meetings (including BPD meetings), EMA Scientific Advice meetings, and written responses to CMC deficiency letters and information requests from global regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide expert regulatory interpretation of FDA and EMA biologics CMC guidance documents and ICH Q-series guidelines applicable to large molecules, including ICH Q8, Q9, Q10, Q11, Q12, and Q13, and advise development teams on process characterization, comparability, and control strategy regulatory acceptability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead post-approval CMC change management strategy for biologics programs, including PACMP development, Prior Approval Supplements (PAS), CBE filings, and EU/global variation submissions related to manufacturing process changes, site changes, and analytical method updates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee regulatory aspects of biologics technology transfer activities, including biosimilar comparability assessments, new CMO site qualification, and regulatory filing strategies for site-to-site manufacturing transfers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide regulatory guidance on biologics-specific CMC considerations, including cell line development, cell banking, upstream and downstream process validation, biophysical and functional characterization, and extended characterization strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to regulatory due diligence evaluations of biologics licensing candidates or acquisition targets, assessing CMC regulatory risk, comparability study adequacy, and submission readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tracks CMC regulatory deliverables and submission timelines across all biologics programs, ensuring proactive identification of dependencies, risks, and upcoming milestones to keep cross-functional teams aligned and submission-ready.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a fully integrated partner within the CMC team, attending key technical meetings, engaging daily with Process Development, Analytical, Manufacturing Sciences, Drug Supply and Quality colleagues, and translating regulatory strategy into practical guidance that enables the CMC team to make informed decisions and move programs forward with regulatory confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate entrepreneurial drive and resourcefulness in executing CMC regulatory responsibilities — proactively seek out information, build relationships across the CMC organization, and find creative avenues to get things done; a successful CMC regulatory lead takes ownership of being plugged in, earns trust within the team, and removes barriers through initiative and ownership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Advanced degree (PhD, MS, or PharmD) in biochemistry, molecular biology, pharmaceutical sciences, immunology, or a related biologics-relevant discipline strongly preferred or equivalent years of experience.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 12+ years of CMC regulatory affairs experience in the pharmaceutical or biotech industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep and comprehensive expertise in biologics CMC regulatory strategy, including cell line development, upstream and downstream process development and validation, biophysical characterization, analytical method validation, and drug product formulation and fill-finish for parenteral biologics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience authoring and overseeing biologics CMC sections of global regulatory submissions, including INDs/CTAs, BLAs, MAAs, and post-approval supplements and variations in ICH CTD/eCTD format.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of leading FDA and EMA biologics CMC Health Authority meetings, including BPD (Biologics Product Development) meetings, pre-BLA meetings, and strategic management of CMC deficiency letter responses\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of ICH Q8/Q9/Q10/Q11/Q12/Q13 guidelines, FDA biologics CMC guidance (including CDER and CBER guidance for therapeutic biologics), and EMA quality guidance applicable to monoclonal antibodies and other biological entities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience managing biologics-specific CMC regulatory challenges, including comparability study strategy, reference standard lifecycle management, specification negotiation, and extended characterization regulatory justification.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead and develop cross-functional teams in a fast-paced, resource-constrained biotech or pharmaceutical environment; fosters a culture of accountability, inclusion, and continuous learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of influencing without authority across organizational boundaries, driving alignment among senior stakeholders, and building consensus on complex regulatory or scientific priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating organizational ambiguity and change; capable of defining structure, establishing priorities, and scaling functional capabilities in alignment with evolving corporate strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional written and verbal communication skills with demonstrated ability to translate complex regulatory, scientific, or operational content for diverse audiences, including executive leadership, Health Authorities, and cross-functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at preparing and delivering compelling presentations, briefing documents, and strategic updates to cross-functional leadership teams, board-level stakeholders, and external regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong active listening skills and the ability to synthesize input from diverse perspectives into clear, actionable communications that build alignment and drive regulatory decision-making.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$242,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$313,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035451009,"name":"Regulatory \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4371398009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4214651009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4371398009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"106","title":"Senior Director, Regulatory Affairs CMC – Small Molecule","company_name":"Beeline Medicines","first_published":"2026-08-16T14:48:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Regulatory Affairs CMC – Small Molecules provides senior-level scientific and strategic regulatory leadership for all Chemistry, Manufacturing, and Controls (CMC) activities related to the company\u0026#39;s small molecule assets within the immunology and inflammation (I\u0026amp;amp;I) portfolio. This role is responsible for developing and executing CMC regulatory strategies from early clinical development through NDA filing and post-approval lifecycle management, serving as the company\u0026#39;s foremost authority on small molecule CMC regulatory science. The Senior Director partners with Technical Development, Process Chemistry, Analytical Sciences, Quality, and external CMOs to ensure that CMC programs are designed, documented, and submitted in full alignment with FDA, EMA, and global Health Authority expectations. As a senior leader within the Regulatory Affairs organization, this individual also contributes to the broader regulatory strategy, and plays a key role in shaping the company\u0026#39;s regulatory affairs infrastructure\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead the CMC regulatory strategy for all small molecule assets in the I\u0026amp;amp;I portfolio, from IND/CTA through NDA filing, including post-approval lifecycle management and labeling strategy for drug substance and drug product.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, review, and oversee the preparation of CMC sections of global regulatory submissions in ICH CTD format, including INDs, CTAs, NDAs, MAAs, Type II variations, and supplements, with accountability for quality, completeness, and regulatory defensibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the company\u0026#39;s primary regulatory authority and strategic partner for small molecule Technical Development, Process Chemistry, Analytical Development, Formulation Sciences, and Quality functions on all CMC regulatory matters.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead Health Authority interactions related to small molecule CMC topics, including FDA Type B and Type C meetings, EMA Scientific Advice meetings, and written responses to CMC deficiency letters and information requests from global regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide expert regulatory interpretation of FDA, EMA, and ICH CMC guidance documents applicable to small molecules, including ICH Q8, Q9, Q10, Q11, and Q12, and proactively advise development teams on design space, process validation, and control strategy regulatory acceptability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead post-approval CMC change management strategy for small molecule programs, including SUPAC assessments, Prior Approval Supplements (PAS), Changes Being Effected (CBE) filings, and ex-US variation submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee regulatory aspects of small molecule technology transfer activities, including new CMO onboarding, site-to-site comparability, and associated regulatory filing updates.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and maintain CMC regulatory SOPs, templates, and document management workflows specific to small molecule programs, ensuring compliance with ICH CTD, eCTD, and applicable electronic submission requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to regulatory due diligence evaluations of small molecule licensing candidates or acquisition targets, providing CMC regulatory risk assessment and readiness analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tracks CMC regulatory deliverables and submission timelines across all small molecule programs, ensuring proactive identification of dependencies, risks, and upcoming milestones to keep cross-functional teams aligned and submission-ready.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a fully integrated partner within the CMC team, attending key technical meetings, engaging daily with Process Development, Analytical, Manufacturing Sciences, Drug Supply and Quality colleagues, and translating regulatory strategy into practical guidance that enables the CMC team to make informed decisions and move programs forward with regulatory confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate entrepreneurial drive and resourcefulness in executing CMC regulatory responsibilities — proactively seek out information, build relationships across the CMC organization, and find creative avenues to get things done; a successful CMC regulatory lead takes ownership of being plugged in, earns trust within the team, and removes barriers through initiative and ownership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Advanced degree (PhD, MS, or PharmD) in organic chemistry, pharmaceutical sciences, analytical chemistry, or a related small molecule-relevant discipline strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 12+ years of CMC regulatory affairs experience in the pharmaceutical or biotech industry preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep and comprehensive expertise in small molecule CMC regulatory strategy, including drug substance (API) synthesis and control, drug product formulation and manufacturing, and analytical method development and validation for oral, parenteral, and other dosage forms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience authoring and overseeing small molecule CMC sections of global regulatory submissions, including INDs/CTAs, NDAs, MAAs, and post-approval supplements and variations in ICH CTD/eCTD format.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of leading FDA and EMA CMC-focused Health Authority meetings, including preparation of briefing documents and strategic management of written responses to CMC deficiency letters\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of ICH Q8/Q9/Q10/Q11/Q12 guidelines, FDA small molecule CMC guidance documents (e.g., SUPAC, process validation, container closure), and EMA quality guidance applicable to small molecule chemical entities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience managing CMC regulatory aspects of technology transfer, new CMO qualification, and site change regulatory filing strategies for small molecule programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong command of post-approval CMC change management regulations, including SUPAC categories, PAS/CBE filing requirements, and ex-US variation frameworks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead and develop cross-functional teams in a fast-paced, resource-constrained biotech or pharmaceutical environment; fosters a culture of accountability, inclusion, and continuous learning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record of influencing without authority across organizational boundaries, driving alignment among senior stakeholders, and building consensus on complex regulatory or scientific priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience navigating organizational ambiguity and change; capable of defining structure, establishing priorities, and scaling functional capabilities in alignment with evolving corporate strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional written and verbal communication skills with demonstrated ability to translate complex regulatory, scientific, or operational content for diverse audiences, including executive leadership, Health Authorities, and cross-functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at preparing and delivering compelling presentations, briefing documents, and strategic updates to cross-functional leadership teams, board-level stakeholders, and external regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adept at facilitating productive dialogue in high-stakes meetings, Health Authority interactions, and multi-party collaborations; balances clarity, diplomacy, and scientific precision\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$242,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$313,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035451009,"name":"Regulatory \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4405169009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4234385009,"location":{"name":"United States"},"metadata":null,"id":4405169009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"137","title":"Senior Director, Regulatory Strategy – Global Regulatory Lead","company_name":"Beeline Medicines","first_published":"2026-09-14T11:19:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Regulatory Strategy – Global Regulatory Lead is responsible for developing and leading the integrated global regulatory strategies for assigned programs in the immunology and inflammation (I\u0026amp;amp;I) therapeutic area, with a particular focus autoimmune indications. This role serves as the primary regulatory strategist and Health Authority relationship lead for assigned programs, guiding development teams in the design of regulatory-sound development plans, optimal filing strategies, and Health Authority engagement. The Senior Director provides a global perspective across FDA, EMA, and other major regulatory jurisdictions, ensuring that regulatory strategy is proactively integrated into all aspects of early clinical and translational development. As a key member of the Regulatory Affairs leadership team, this individual also contributes to the development of the company\u0026#39;s regulatory infrastructure, capabilities, and organizational best practices for program oversight.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Remote - \u0026lt;/strong\u0026gt;This position is designated as remote; the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company\u0026#39;s discretion based on business need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and lead integrated global regulatory strategies for assigned pipeline programs in the I\u0026amp;amp;I portfolio, encompassing pre-IND planning, IND/CTA submission strategy, Phase I/II/III development planning, and regulatory pathway optimization across major global jurisdictions including FDA, EMA, PMDA, and others.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary regulatory strategist for assigned program teams, providing expert guidance on development plan design, regulatory risk identification, filing sequencing, and Health Authority engagement strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the preparation and execution of regulatory meetings, including management of timelines, briefing document development, strategic meeting preparation, and agency interaction management; translate Health Authority feedback into actionable development recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain integrated regulatory development plans (iRDPs) and regulatory timelines for all assigned programs, ensuring alignment with clinical, CMC, and non-clinical development activities and overall program milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead IND, CTA, NDA and BLA submissions, regulatory planning and submission of pediatric development plans.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic input to clinical protocols, non-clinical study designs, and early CMC development activities to ensure regulatory acceptability and alignment with global development strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and interpret evolving FDA and global regulatory guidance, precedent regulatory decisions, and competitive landscape intelligence relevant to I\u0026amp;amp;I development programs and proactively integrate insights into pipeline regulatory strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Evaluate and leverage expedited regulatory pathway opportunities for pipeline programs, including Breakthrough Therapy Designation (BTD), Fast Track Designation, PRIME designation (EMA), and Orphan Drug Designation where applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory Affairs CMC, Clinical Development, Non-Clinical Sciences, Bioanalytics, and Translational Sciences teams to ensure that cross-functional development activities are regulatory-strategy aligned from the earliest stages of development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to regulatory due diligence activities for pipeline asset evaluations, in-licensing candidates, and business development targets, assessing regulatory risk profiles, development pathway viability, and filing readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain appropriate trackers of regulatory activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Concise, clear and frequent communication with cross functional team. This position requires maturity, finesse and leadership to lead the cross-functional team, and high level of strategic acumen and finesse to define and lead regulatory interactions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess resource needs to support the assigned programs and with manager, participate in the development of the budget for assigned programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Advanced degree (PhD, PharmD, or master\u0026#39;s level) in a relevant life sciences discipline required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 12+ years of regulatory affairs experience in the pharmaceutical or biotech industry preferred, with at least 5–7 years of direct responsibility for global regulatory strategy leadership on clinical development programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in global regulatory strategy development for biologics and/or small molecule therapeutics, with demonstrated experience developing regulatory plans across FDA, EMA, and additional global jurisdictions from pre-IND through post approval.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience preparing and leading Health Authority interactions, including FDA pre-IND, Type B, and Type C meetings and EMA Scientific Advice meetings, with a strong track record of productive agency relationships and strategic translation of feedback.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge of FDA regulations (21 CFR Parts 312 and 314/601), EMA regulatory frameworks, ICH E8(R1), ICH E9(R1), and applicable guidance documents relevant to early clinical development in I\u0026amp;amp;I or autoimmune disease indications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in immunology, inflammation, autoimmune disease, or a related therapeutic area is strongly preferred; knowledge of lupus regulatory landscape and precedent regulatory decisions is a meaningful advantage.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic thinking skills, intellectual curiosity, and the ability to synthesize complex scientific and regulatory information into clear, actionable regulatory development recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to operate independently, driving execution of regulatory plans with agility and efficiency, while exercising sound judgment in stakeholder engagement, including proactively keeping leadership appropriately informed and involving senior management at key decision points.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to manage multiple concurrent priorities with focus, efficiency, and sound judgment, balancing competing timelines and development milestones in a matrix biotech organization, with an appreciation for the visibility and criticality of programs in a small-company environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional written and verbal communication skills with demonstrated ability to translate complex regulatory, scientific, or operational content for diverse audiences, including executive leadership, Health Authorities, and cross-functional partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to communicate operational information into clear, actionable insights, providing decisive direction to teams and driving efficient, aligned execution across functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled at preparing and delivering compelling presentations, briefing documents, and strategic updates to cross-functional leadership teams, board-level stakeholders, and external regulatory agencies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adept at facilitating productive dialogue in high-stakes meetings, Health Authority interactions, and multi-party collaborations; balances clarity, diplomacy, and scientific precision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong active listening skills and the ability to synthesize input from diverse perspectives into clear, actionable communications that build alignment and drive regulatory decision-making.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$242,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$313,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035451009,"name":"Regulatory \u0026 Quality","child_ids":[],"parent_id":null}],"offices":[{"id":4036151009,"name":"Remote (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4439435009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4256772009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4439435009,"updated_at":"2026-10-23T09:46:01-04:00","requisition_id":"154","title":"Senior Executive Assistant \u0026 Office Operations","company_name":"Beeline Medicines","first_published":"2026-10-08T18:43:00-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;The Senior Executive Assistant \u0026amp;amp; Office Operations is a highly trusted, senior-level partner responsible for providing exceptional executive support to senior leaders and members of the Research \u0026amp;amp; Development organization while also partnering on key office operations for the Boston location. This role supports a globally distributed leadership team and partners closely with the Senior Executive Assistant to the Chief Medical Officer (CMO) and the Research \u0026amp;amp; Development Leadership Team (RDLT) to coordinate high-priority activities, leadership meetings, and strategic initiatives.\u0026lt;/span\u0026gt;\u0026lt;span data-ccp-props=\u0026quot;{\u0026amp;quot;201341983\u0026amp;quot;:0,\u0026amp;quot;335559738\u0026amp;quot;:0,\u0026amp;quot;335559739\u0026amp;quot;:100,\u0026amp;quot;335559740\u0026amp;quot;:240}\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition to executive support, this role serves as the primary owner of office operations and facilities management for the Boston location, partnering closely with the Director, Corporate \u0026amp;amp; Administrative Services on workplace planning, construction, branding initiatives, and employee experience. This position is part of Beeline Medicines’ broader Executive Assistant team and is expected to flex in supporting firmwide priorities and events.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span data-contrast=\u0026quot;auto\u0026quot;\u0026gt;The ideal candidate is a polished, poised, and highly resourceful professional who excels in fast-paced biotechnology environments. They demonstrate exceptional judgment, executive presence, discretion, and the ability to quickly assess competing priorities. Success in this role requires someone who can rapidly learn organizational dynamics, understand the relative importance and urgency of meeting requests, and confidently manage complex scheduling challenges while maintaining a high level of professionalism\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as\u0026amp;nbsp;\u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provides dedicated support to the assigned executives and works closely with assigned functional departments across the organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide proactive, high-level executive support, managing complex calendars, travel, expenses, and rapidly evolving priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with the Senior Executive Assistant to the CMO and the RDLT to coordinate leadership meetings, strategic planning sessions, governance forums, and other high-priority engagements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exercise sound judgment in prioritizing meeting requests and managing competing executive demands, ensuring leadership time is aligned with organizational priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage complex calendaring across multiple global time zones and facilitate coordination among internal and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and coordinate domestic and international travel, including multi-stop itineraries, executive briefings, and contingency planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support executive interactions with key external stakeholders, advisors, investigators, and partners, including scheduling, logistics, preparation, and follow-up.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a trusted partner who anticipates needs, identifies potential conflicts, and proactively recommends solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate office and pantry supplies, maintaining appropriate inventory levels and employee amenities in partnership with the Senior Executive Assistant.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review office and facilities-related expenses and identify opportunities for operational efficiencies and cost optimization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner on facilities matters, including maintenance requests, vendor relationships, building management coordination, and work orders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as an engaged and collaborative member of the Executive Assistant team, supporting company-wide initiatives and shared priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support logistics and planning for town halls, leadership meetings, all-hands meetings, company events, employee engagement activities, company-wide mailings, and cross-functional initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate flexibility and willingness to support evolving business needs and organizational priorities.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelor\u0026#39;s degree or equivalent professional experience required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 15 years of experience supporting Csuite executives and senior leadership teams in fast paced, global environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in biotechnology or life sciences strongly preferred; R\u0026amp;amp;D or clinical development experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to support multiple senior leaders simultaneously with discretion, professionalism, and confidence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience working across global time zones and supporting internationally based executives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting industry congresses, scientific meetings, and senior level external engagements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced proficiency in Microsoft Office suite, including Outlook, Word, Excel, and PowerPoint.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with DocuSign, SharePoint, Coupa, SAP, and Concur or comparable expense management platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong command of video conferencing and collaboration tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable adopting new technologies; familiarity with AI-enabled productivity tools such as Microsoft Copilot is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Operates with a high degree of autonomy and ownership, functioning as a trusted extension of executive leadership in both internal and external settings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipates organizational needs before they surface, proactively identifying risks, gaps, and opportunities to keep executive priorities on track.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-directed and confident, with the ability to orient quickly in ambiguous or fast-moving environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicates with clarity, precision, and discretion across all levels of the organization, tailoring style and tone to audience and context.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Navigates sensitive information with professionalism and strict confidentiality, exercising discretion in all written and verbal interactions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly effective interpersonally; able to build trusted relationships with executives, cross-functional teams, vendors, and external partners.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$113,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$146,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035456009,"name":"Administrative Services","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4470187009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4287119009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4470187009,"updated_at":"2026-10-27T19:14:34-04:00","requisition_id":"158","title":"Senior Medical Affairs Operations Manager","company_name":"Beeline Medicines","first_published":"2026-10-27T19:14:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Director, Medical Operations, the Senior Manager, Medical Operations, leads project management and operational execution for Medical Affairs initiatives that support the function’s growth and strategy. They will bring medical affairs expertise and strong project management skills to build project plans, manage budgets, and deliver key milestones on time.\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As a central point of coordination, you will partner with Scientific Communications, Patient Advocacy, Clinical Development, and Field Medical leaders to keep communication clear and collaboration effective. Success in this role requires a solid understanding of medical affairs, disciplined execution, and strategic thinking. This role supports the planning and delivery of global Medical Affairs initiatives, including KOL engagement, congress execution, medical education efforts, and cross-functional coordination.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Essential Duties and Responsibilities:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead operational planning and budget tracking for Medical Affairs programs, including MSL field activities and medical education\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage vendor relationships, contracts, purchase orders, and invoicing for Medical Affairs initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain Medical Affairs SOPs, training materials, and compliance processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate advisory boards, congress activities, and medical education program logistics with cross-functional partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support onboarding and training of new Medical Affairs team members on systems and processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with grant/donation and investigator-sponsored research (ISR) request tracking and review coordination.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to continuous improvement of medical affairs operational workflows.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and report key performance indicators (KPIs) to Medical Affairs leadership, highlighting risks and opportunities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the operational liaison between Medical Affairs, Legal, and Finance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelors Degree in related scientific, business or other related discipline required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of medical affairs operations, program management, or related experience in the pharma/biotech industry.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with Medical Affairs CRM and content management systems (e.g., Veeva).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of medical affairs compliance requirements related to grants, donations, and speaker programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with reporting and dashboarding tools used to track program KPIs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage cross-functional projects and vendors with minimal supervision.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment in prioritizing competing operational demands across programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to identify process gaps and drive improvements without waiting for direction.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong written and verbal communication skills for coordinating across Medical Affairs, Compliance, and Finance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to clearly summarize budget and program status for departmental leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at coordinating logistics and expectations with external vendors and speakers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 10%+ as needed of time or more including occasional overnight stay driven by business need\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$165,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$214,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4324982009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4190157009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4324982009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"94","title":" Senior Medical Director, Clinical Development","company_name":"Beeline Medicines","first_published":"2026-07-20T21:06:08-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Medical Director, Clinical Development is a senior physician-scientist who provides strategic medical leadership for one or more clinical programs within the organization’s Inflammation \u0026amp;amp; Immunology pipeline. Building on deep therapeutic area expertise and a proven track record in clinical trial execution, this role bridges hands-on clinical program leadership with broader cross-functional and organizational accountability. The Senior Medical Director serves as the primary physician lead for assigned assets, owning the clinical strategy and development plan across multiple phases, while also playing an increasingly prominent role in shaping departmental capabilities, mentoring junior physicians, and contributing to portfolio-level decision-making. This role requires the ability to work with independence and authority in a fast-paced, growth-stage biopharmaceutical environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the physician medical lead for assigned clinical development programs — owning the clinical development strategy, integrated development plan, and medical decision-making for pipeline assets across Phase I through Phase III development, with increasing accountability for program-level outcomes and portfolio contributions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the design, authorship, and review of clinical trial protocols, investigator brochures, informed consent documents, and clinical sections of regulatory submissions (IND, NDA/BLA, global filings) — ensuring scientific rigor, patient safety, and regulatory compliance across all deliverables.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide comprehensive medical oversight of ongoing clinical trials — including safety monitoring, medical monitoring, SAE assessment, protocol deviation review, and benefit-risk evaluation — in close partnership with Clinical Operations, Pharmacovigilance, and Biostatistics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and actively represent the organization in regulatory agency interactions — including FDA and EMA meetings, briefing document development, and responses to health authority questions — serving as a primary medical spokesperson for assigned programs and contributing to regulatory strategy.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support pharmacovigilance activities during trial conduct — Drive cross-functional clinical program teams as the senior medical lead — providing strategic scientific direction to Clinical Operations, Regulatory Affairs, Translational Medicine, Biostatistics, and Medical Affairs — and ensure integrated, high-quality program execution with clear accountability and pace.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain relationships with key opinion leaders (KOLs), principal investigators, and academic medical centers to strengthen the organization’s clinical network, gather external scientific insights, and support the medical positioning of pipeline assets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Advanced clinical degree (MD or DO) required. Board certification or clinical training in rheumatology, nephrology, immunology, or a related specialty strongly preferred. Additional advanced degree (PhD, MPH, or MBA) is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 10 years of combined clinical and pharmaceutical/biotech industry experience, with a minimum of 5 years in a clinical development role with increasing levels of responsibility preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep scientific expertise in autoimmune disease — rheumatology preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience as a physician lead on Phase I–III clinical programs, including hands-on protocol development, medical monitoring, and regulatory submission experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep clinical and scientific expertise in immunology and inflammation— including command of disease mechanisms, clinical trial landscapes, standard of care evolution, regulatory developments, and emerging therapeutic approaches\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to identify, characterize, and mitigate clinical, operational, and regulatory risks across multi-site, multinational clinical programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to serve as the senior medical authority on cross-functional program teams — setting scientific direction, resolving complex medical questions, and building alignment across diverse functional stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong track record of leading clinical programs through critical milestones — including first-in-human studies, proof-of-concept readouts, pivotal trial initiation, and regulatory submissions — with a bias for rigor, speed, and quality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at delivering data-driven recommendations to senior leadership, adapting communication to drive informed decision-making at the organizational and portfolio level\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative and influential leader who builds trust and credibility with clinical investigators, KOLs, and regulatory agencies — leveraging scientific expertise and interpersonal effectiveness to advance the organization’s programs and reputation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional scientific and medical communication skills — able to present complex clinical data, safety findings, and development strategies clearly and compellingly to diverse audiences including regulators, investigators, executives, and patient communities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled in authoring and reviewing high-quality clinical documents including protocols, investigator brochures, clinical study reports, regulatory briefing documents, and scientific manuscripts\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$293,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$379,500 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035446009,"name":"Clinical Development","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4422011009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4244660009,"location":{"name":"Cambridge, Massachusetts, United States"},"metadata":null,"id":4422011009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"148","title":"Senior Medical Director, Medical Affairs","company_name":"Beeline Medicines","first_published":"2026-09-26T18:00:45-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Medical Director, Medical Affairs is a senior therapeutic and disease area expert who serves as the organization\u0026#39;s primary external medical and scientific resource for healthcare providers (HCPs), key medical experts (KMEs), clinical investigators, healthcare plans, hospital formulary decision-makers, and patient advocacy organizations. This role operates at the intersection of scientific leadership and external engagement — building and sustaining trusted peer-level relationships within the I\u0026amp;amp;I community while driving the development and execution of the organization\u0026#39;s medical affairs strategy most notably for the Beeline Medicines lead program; an investigational selective, oral, once-daily TLR7/8 inhibitor advancing into pivotal development for systemic and cutaneous lupus erythematosus — and for the broader I\u0026amp;amp;I portfolio. The Senior Medical Director leads scientific exchange, supports evidence generation, shapes medical education and KME engagement programs, and serves as a senior internal scientific authority — providing medical input to clinical development, commercial readiness, market access, and regulatory strategy. \u0026amp;nbsp;The Senior Medical Director also serves as a medical reviewer and signatory on the promotional and medical review (MLR) committee for all externally facing company materials for health care professionals, advocacy groups and allied health care functions globally, ensuring factual accuracy and compliance with industry codes of conduct and regulations \u0026amp;nbsp;Reporting to the SVP of Clinical Development and Medical Affairs, this individual brings deep scientific expertise in autoimmune disease, demonstrated KME relationship management, and the strategic leadership presence required to drive the medical affairs function forward in a clinical-stage, resource-efficient biotech environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary medical and scientific point of contact for KMEs, clinical investigators, HCPs, healthcare plan decision-makers, and patient advocacy groups within the I\u0026amp;amp;I therapeutic area — with a primary focus on lupus (SLE and CLE) across rheumatology, dermatology, and nephrology — building and sustaining trusted, peer-level relationships that advance the organization\u0026#39;s scientific and medical objectives. The Senior Medical Director may also support other therapeutic areas as required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and lead the execution of the medical affairs strategy for the I\u0026amp;amp;I pipeline, including lupus indications — encompassing KME engagement, evidence generation, medical education, advisory board programming, and publication strategy — in alignment with clinical development milestones and corporate goals.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and conduct peer-to-peer scientific exchange with KMEs, investigators, and HCPs — sharing clinical and emerging data, discussing unmet medical needs, and gathering external insights that inform medical strategy, pipeline positioning, and commercial readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and critically assess competitive clinical data and emerging mechanisms to inform differentiation and scientific positioning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Scientific Communications to develop and maintain the core scientific narrative, medical communications platform, and scientific lexicon; including unbranded disease-state and mechanism-of-action education to build external scientific understanding of a novel target ahead of pivotal readouts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the design and execution of medical advisory board meetings — identifying and engaging the right scientific experts, developing scientifically rigorous agendas, and ensuring that advisory board insights translate into actionable medical and strategic recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee the development and review of medical content — including medical education materials, scientific slide decks, congress abstracts, posters, and manuscripts — ensuring scientific accuracy, regulatory compliance, and strategic alignment across all external communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Scientific Communications to develop and execute data disclosure and publication plans as executed in accordance with GPP 2022 and ICMJE authorship criteria.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead scientific engagement strategy for major rheumatology congresses, including KME interactions, data communication planning, and insight capture.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Medical Affairs support for clinical programs, including investigator and site identification, feasibility input, engagement of steering committee members and national coordinating investigators, scientific input to protocol design, and site-facing scientific training in partnership with Clinical Development and Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Field Medical Affairs and MSL teams to ensure accurate, balanced, and up-to-date scientific tools and resources are available and consistently applied in field engagements — participating directly in key field interactions when the scientific complexity or stakeholder importance warrants senior medical presence.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic medical input into data generation initiatives including interventional (phase 3b, 4) and non-interventional trial design (real world evidence approaches, registry studies) to support market authorization of the asset and life cycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Clinical Development, Biostatistics, Regulatory Affairs, and other departments on the medical interpretation of clinical data, regulatory submissions, payer engagement strategies, and commercial launch planning — serving as a medical affairs voice across all key cross-functional initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Advanced clinical degree (MD or DO) required. Board certification or clinical training in rheumatology, dermatology, nephrology, immunology, or a related specialty strongly preferred. Additional advanced degree (PhD, MPH, or MBA) is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 5 years clinical and 5 years pharmaceutical/biotech industry experience in medical affairs inclusive of supporting product launches preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience managing or advising lupus clinical programs strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep scientific expertise in autoimmune disease — specifically lupus (SLE and/or CLE), rheumatology, and/or nephrology — required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Established KME network within the lupus, rheumatology, and dermatology communities strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting a registrational or pivotal program through pre-launch medical affairs readiness — including major congress data disclosure, field medical build-out, and compliant pre-approval payer engagement — strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep clinical and scientific expertise in immunology and inflammation — with primary depth in lupus nephritis, SLE, and/or CLE — including command of disease mechanisms, clinical trial landscapes, standard of care evolution, regulatory developments, and emerging therapeutic approaches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to critically evaluate, synthesize, and communicate complex clinical and scientific literature — including clinical trial data, real-world evidence, and regulatory data packages — to diverse internal and external audiences.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting regulatory submissions, label negotiations, or advisory committee preparations from a medical affairs perspective; familiarity with promotional review processes and compliance frameworks governing medical communications.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working command of the compliance framework governing pre-approval scientific exchange — medical–commercial separation, non-promotional communication standards, reactive-only handling of unapproved-use inquiries, the PhRMA Code, FDA OPDP guidance, and applicable EFPIA/ABPI codes — together with transparency obligations including Open Payments reporting of transfers of value.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience with advisory board design, scientific meeting planning, ISR program oversight, HEOR strategy, and external expert relationship management in a pharmaceutical or biotech medical affairs context.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Senior medical affairs leader with demonstrated ability to define and execute medical strategy, lead cross-functional medical initiatives, and operate with significant independence in a lean, clinical-stage biotech environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven external relationship leader — builds and sustains trusted, long-term relationships with national and regional KMEs, clinical investigators, and patient advocacy organizations through scientific credibility, consistent follow-through, and genuine commitment to advancing medical knowledge.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Influential cross-functional partner — drives alignment across Medical Affairs, Clinical Development, Regulatory, Commercial, and Market Access through strong scientific authority and the ability to translate medical insights into organizational action via clear, prioritized medical actions and strategic recommendations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional scientific and medical communicator — engages KMEs, investigators, HCPs, payers, and patient advocacy leaders in substantive, peer-level scientific dialogue with depth, balance, and clarity appropriate to each audience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Skilled presenter and medical content developer — prepares and delivers compelling presentations, advisory board materials, and scientific updates to external experts, cross-functional leadership, and executive audiences with precision and strategic framing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong active listener and external insights integrator — synthesizes KME perspectives, clinical practice trends, and competitive intelligence into actionable medical strategy recommendations that inform organizational decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 30%+ as needed of time or more including occasional overnight stay driven by business need\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relocation available\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$293,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$345,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4034861009,"name":"Cambridge, MA Office","location":"Cambridge, Massachusetts, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4470123009","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":4287078009,"location":{"name":"Durham, North Carolina, United States"},"metadata":null,"id":4470123009,"updated_at":"2026-10-27T18:13:48-04:00","requisition_id":"157","title":"Senior Outsourcing Manager","company_name":"Beeline Medicines","first_published":"2026-10-27T18:13:48-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Outsourcing Manager, within the Procurement \u0026amp;amp; Outsourcing department, will lead outsourcing and vendor management activities across R\u0026amp;amp;D, with a strong focus on Clinical Development and related functions. This role serves as a key partner to Clinical, R\u0026amp;amp;D, Tech Ops, Finance, and other stakeholders, supporting vendor strategy, selection, contracting, governance, financial planning and reporting, and ongoing performance management.\u0026amp;nbsp;The Senior Outsourcing Manager will manage vendor relationships throughout the engagement lifecycle, helping teams proactively address performance, budget, scope, and operational risks. The role will also support functional department contracts and associated financial planning, forecasting, budget tracking, and reporting activities, helping ensure appropriate visibility into vendor spend, commitments, and changes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;In addition, the role will support key procurement activities, including RFPs, vendor negotiations, contracting, and onboarding, while ensuring alignment with internal SOPs, procurement policies, and business objectives.\u0026amp;nbsp;Success in this role is measured by strong vendor partnerships, effective financial and performance oversight, proactive issue resolution, and the ability to support program and functional teams as business priorities evolve\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage outsourced vendor relationships across R\u0026amp;amp;D and Clinical programs, providing ongoing oversight of scope, budget, performance, timelines, risks, and contractual commitments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical, R\u0026amp;amp;D, Tech Ops, Finance, and functional teams to support outsourcing strategy, vendor selection, contracting, financial planning, and ongoing vendor management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support vendor governance activities, including performance reviews, KPI/scorecard management, financial reviews, issue escalation, risk management, and follow-up of key actions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support program and functional department financial planning and reporting, including vendor forecasts, budget tracking, accruals, commitments, change orders, and variance analysis.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage functional department contracts and vendor engagements, partnering with business owners to ensure appropriate scope, budget, contractual coverage, and financial visibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain vendor qualification, performance scorecards, risk assessments, and other oversight tools for outsourced partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and negotiate investigative site contracts, including budgets and exhibits, in partnership with Legal and Clinical.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead select end-to-end sourcing events (RFI/RFP/RFQ) for program teams, functional departments, and corporate needs, including CRO, laboratory, and professional services vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate master service agreements, statements of work, change orders, and commercial terms in partnership with Legal, Finance, and business stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support procurement and financial systems and processes, ensuring accurate and timely vendor, contract, purchase order, and financial data.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and report on purchase orders and invoices, including PO balances, invoice status, spend against commitments, and reconciliation of discrepancies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track procurement and financial issues through resolution, partnering with Finance, Accounts Payable, vendors, and internal stakeholders to address PO, invoice, payment, and system-related issues.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain procurement and outsourcing reporting to provide visibility into vendor spend, contractual commitments, PO utilization, forecasts, and other key metrics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support supplier onboarding, due diligence, and ongoing compliance monitoring in accordance with company policies and applicable SOPs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities to improve vendor value, cost management, contracting efficiency, financial visibility, and outsourcing/procurement processes across the organization.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform the other assigned duties and responsibilities as assigned.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education:\u0026amp;nbsp;Bachelor\u0026#39;s degree in Business, Supply Chain Management, Finance, or a related field required.\u0026amp;nbsp;MBA or relevant advanced degree/certification (e.g., CPSM, CIPS) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5 years of outsource management, procurement, contracting and vendor management experience, ideally within biotech/pharma or a CRO-facing environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with procurement/contract management systems (e.g., Coupa, Ariba, SAP).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong command of Excel-based spend analysis, benchmarking, and reporting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to influence stakeholders and drive sourcing decisions without direct authority.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment in balancing cost, quality, and speed trade-offs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage competing priorities across multiple concurrent sourcing initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive in identifying risk and escalating issues before they impact the business\u0026lt;strong\u0026gt;.\u0026lt;/strong\u0026gt;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong negotiation and vendor relationship management skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear written and verbal communication with internal stakeholders and external suppliers.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to present sourcing recommendations and business cases to leadership.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$124,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$160,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035459009,"name":"Accounting","child_ids":[],"parent_id":null}],"offices":[{"id":4038675009,"name":"Durham, NC Office","location":"Durham, North Carolina, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4329259009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4193241009,"location":{"name":"Stamford, Connecticut, United States"},"metadata":null,"id":4329259009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"96","title":"Staff Accountant","company_name":"Beeline Medicines","first_published":"2026-07-22T21:56:04-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Staff Accountant is a foundational member of Accounting team, responsible for supporting the day-to-day accounting operations, monthly close process, and financial reporting activities of a clinical-stage biotech. This role provides accurate and timely accounting support across general ledger maintenance, accounts payable, account reconciliations, and expense reporting — contributing to the integrity of the financial records that underpin the organization\u0026#39;s reporting and compliance obligations. Operating in a lean finance environment, the Staff Accountant is expected to bring attention to detail, a strong work ethic, and a genuine desire to build foundational accounting skills in a fast-paced, high-growth life sciences setting. This is an excellent opportunity for an early-career accounting professional to gain broad exposure to all aspects of biotech accounting and develop their skills alongside an experienced Finance team.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Hybrid - \u0026lt;/strong\u0026gt;This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as \u0026lt;strong\u0026gt;Tuesday and Wednesday\u0026lt;/strong\u0026gt;. Additional on-site days may be required based on business needs, team priorities, or leadership direction.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support the monthly financial close process — preparing and posting journal entries, performing account reconciliations, and assisting with the preparation of close workpapers across assigned accounting areas including prepaid expenses, accruals, and fixed assets.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process and manage accounts payable activities — reviewing and coding vendor invoices, coordinating approval workflows, maintaining vendor records, and supporting timely and accurate payment processing in accordance with company policies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare and maintain accounting schedules and supporting documentation for assigned balance sheet accounts — ensuring all reconciliations are completed accurately, on schedule, and supported by appropriate backup documentation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical and research program accrual processes — working with Clinical Operations, Finance, and external vendors to track program expenditures, estimate accruals, and ensure accurate recording of CRO and research-related costs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in the preparation of external audit support — organizing workpapers, preparing schedules, and gathering documentation in response to auditor requests under the direction of the Manager, Accounting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support accounts payable vendor management — maintaining accurate vendor master data, processing new vendor setups, and ensuring W-9/W-8 compliance in coordination with Tax and Finance leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the continuous improvement of accounting processes — identifying opportunities to streamline workflows, improve documentation standards, and enhance the efficiency of close and reporting activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Bachelor\u0026#39;s degree in Accounting or Finance required. CPA exam eligibility or active progress toward CPA licensure preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3 years of accounting experience in a corporate, public accounting, or life sciences environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;to general ledger accounting, accounts payable, or financial close processes preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Life sciences or biotech experience is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foundational knowledge of US GAAP accounting principles — including accrual accounting, reconciliation preparation, journal entry documentation, and basic financial statement concepts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in Microsoft Excel — including the ability to prepare and maintain accounting schedules, reconciliations, and supporting workpapers; experience with VLOOKUP, pivot tables, and basic financial formulas.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with accounting software or ERP systems (e.g., NetSuite, QuickBooks, or equivalent); willingness to learn and develop proficiency in the organization\u0026#39;s financial systems.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and organizational skills — able to manage multiple accounting tasks simultaneously, meet close deadlines consistently, and maintain accurate and organized financial records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reliable and accountable team contributor — consistently meets deadlines, follows through on assigned responsibilities, and communicates proactively when issues or questions arise.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process-minded and improvement-oriented — looks for opportunities to work more efficiently, maintain better documentation, and contribute to a higher-quality accounting close process over time.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clear and professional written and verbal communicator — able to correspond with vendors, internal stakeholders, and Finance team members in a professional, organized, and timely manner.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative and responsive — responds to questions and requests from the Finance team, external auditors, and cross-functional partners in a timely, professional, and helpful manner.\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$77,000\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;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4035459009,"name":"Accounting","child_ids":[],"parent_id":null}],"offices":[{"id":4034862009,"name":"Stamford, CT Office","location":"Stamford, Connecticut, United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null},{"absolute_url":"https://job-boards.greenhouse.io/beelinemedicines/jobs/4436732009","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":true}],"internal_job_id":4255204009,"location":{"name":"United States"},"metadata":null,"id":4436732009,"updated_at":"2026-10-08T13:15:46-04:00","requisition_id":"151","title":"Vice President, Medical Affairs","company_name":"Beeline Medicines","first_published":"2026-10-07T11:19:27-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;About Beeline Medicines:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Job Summary:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Vice President, Medical Affairs leads implementation of Medical Affairs strategy across the product portfolio, setting direction for pre- and post-launch activities and ensuring effective engagement with the medical and scientific community throughout the product lifecycle. This role has oversight - of Field Medical Affairs (the Medical Science Liaison organization); Medical Affairs Program Leads; Epidemiology \u0026amp;amp; Real-World Evidence; Medical Operations, Scientific Affairs and Patient Advocacy. The VP partners closely with Clinical Development, Regulatory, and other departments on cross-functional launch planning, data generation strategy and life cycle management; as well as ensuring all external engagements with HCPs, advocacy groups and allied health care functions globally are compliant with industry country codes of conduct and regulations. \u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Work Arrangement \u0026amp;amp; Location:\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Remote -\u0026amp;nbsp;\u0026lt;/strong\u0026gt;This position is designated as remote; the incumbent will be expected to travel to Beeline Medicines’ offices on a periodic basis to support in-person collaboration, team engagement, and business operations. The frequency and scheduling of such visits will be determined at the company\u0026#39;s discretion based on business need.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Essential Duties and Responsibilities: \u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide input and lead implementation of the medical affairs strategy across the product portfolio, including pre- and post-launch activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Development and oversight of HCP engagement strategy, interactions, advisory boards and consulting activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identification of data generation needs and development of appropriate strategies (i.e. phase 3b, 4, real world evidence approaches) for products both in development and as part of life cycle management activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide technical opinion, appraisal and oversight of sponsored research agreements and investigator initiated trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review and provide recommendations at relevant governance forums for grants and sponsorship requests; as well as provide oversight of relevant processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Development, Regulatory, Commercial, and Market Access on cross-functional launch and lifecycle planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, lead, and develop the medical affairs function ensuring relevant processes and tools are in place for effective execution of medical strategy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure all activities within the medical affairs group comply with applicable laws, regulations, and industry codes of conduct inclusive of review and final approval for external company facing materials with HCPs and allied professionals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent Field Medical and Epidemiology/RWE in due diligence and business development activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior scientific spokesperson at external congresses and with healthcare stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties and responsibilities as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;br\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Education: Doctoral degree (MD, DO, Ph.D, PharmD, etc.) required; Medical Degree (MD or DO) board certification in immunology, rheumatology, internal medicine, or a related specialty, with clinical experience in autoimmune disease is strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive Medical Affairs leadership in pharmaceutical and/or biotechnology industry.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;5+ years managing multiple teams and/or functions (e.g., MSLs, RWE, medical information) at the director level or above.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience building, scaling, and matrix Medical Affairs organization including leading global MSL/field medical teams and data generation activities across multiple therapeutic programs and product launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with label-enabling Phase 3b and 4 trial design and execution required, with a demonstrated track record of successful interactions with global health authorities (e.g., FDA, EMA, PMDA, CDE).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Global medical affairs experience preferred, including familiarity with cross-regional regulatory and commercial dynamics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing a medical affairs budget and/or team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep knowledge of medical affairs compliance frameworks (e.g., PhRMA Code, OIG guidance) applicable to field medical and RWE activities required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of field medical operations, KOL engagement models, and advisory board execution required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of real-world evidence generation, and observational and interventional study design and execution required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven executive leadership skills, including building and scaling medical affairs functions, required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strategic thinking with the ability to align medical affairs strategy with broader corporate objectives required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to drive alignment with adjacent functions without direct reporting authority over them required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound judgment balancing scientific integrity, compliance, and commercial considerations required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional communication and relationship-building skills with KOLs, internal leadership, and external stakeholders required.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Position may require ability to travel 30%+ as needed of time or more including occasional overnight stay driven by business need\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relocation available\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;description\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Salary Range:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;p1\u0026quot;\u0026gt;\u0026lt;span data-teams=\u0026quot;true\u0026quot;\u0026gt;The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;title\u0026quot;\u0026gt;Salary Range\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;pay-range\u0026quot;\u0026gt;\u0026lt;span\u0026gt;$322,000\u0026lt;/span\u0026gt;\u0026lt;span class=\u0026quot;divider\u0026quot;\u0026gt;\u0026amp;mdash;\u0026lt;/span\u0026gt;\u0026lt;span\u0026gt;$382,000 USD\u0026lt;/span\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Benefits:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Competitive health and wellness coverage (structure and premiums vary by country)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Paid time off, public holidays, and additional leave entitlements in accordance with local requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Flexible work arrangements / hybrid schedule\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Equal Employment Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;\u0026lt;strong\u0026gt;Reasonable Accommodation:\u0026lt;/strong\u0026gt;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Privacy\u0026lt;/span\u0026gt;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;/strong\u0026gt;Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at \u0026lt;a href=\u0026quot;https://beelinemedicines.com/privacy-policy/\u0026quot;\u0026gt;Privacy Policy - Beeline Medicines\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4069616009,"name":"Medical Affairs","child_ids":[],"parent_id":null}],"offices":[{"id":4036151009,"name":"Remote (US)","location":"United States","child_ids":[],"parent_id":null}],"ai_disclaimer":null,"include_ai_disclaimer":null,"ai_opt_out_request_url":null}],"meta":{"total":29}}