Associate Director, Pharmacovigilance Scientist

About Beeline Medicines 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. Job Summary The Associate Director, Pharmacovigilance Scientist is a medically and scientifically trained pharmacovigilance professional responsible for providing expert scientific and medical oversight of the company's global drug safety activities. This role conducts and oversees signal detection, benefit‑risk assessment, medical case review, and aggregate safety analyses in support of the company's I&I clinical programs and post‑marketing safety obligations. The Associate Director partners with PV Operations, Clinical Development, Medical Affairs, and Regulatory Affairs to ensure that safety information is evaluated rigorously, communicated clearly, and acted upon in a timely and compliant manner. Work Arrangement & Location Hybrid – This position follows a hybrid work schedule, requiring a minimum of two (2) days on‑site per week – currently designated as Tuesday and Wednesday. Additional on‑site days may be required based on business needs, team priorities, or leadership direction. Essential Duties And Responsibilities Serve as the scientific and medical expert for pharmacovigilance activities across the company's I&I pipeline, providing medical case review and clinical assessment of individual adverse event reports and aggregate safety data. Lead and oversee signal detection activities, including routine data mining of the safety database, evaluation of disproportionality analyses, and systematic literature review for emerging safety signals. Conduct benefit‑risk assessments for emerging safety signals and contribute to regulatory responses, labeling updates, and risk management strategies based on scientific evaluation. Author and oversee the scientific content of periodic safety reports, including DSURs, PSURs/PBRERs, PADERs, and line listings, ensuring accurate medical interpretation of safety data. Review and provide medical oversight of ICSR reports, including complex and medically significant cases, ensuring narrative quality, appropriate medical coding, and regulatory compliance. Collaborate with Clinical Development on safety monitoring activities, DSMB materials, safety sections of clinical protocols, Investigator Brochures (IBs), and Clinical Study Reports (CSRs). Partner with Regulatory Affairs on safety labeling strategy, Core Data Sheet (CDS) maintenance, and preparation of written responses to Health Authority safety queries. Contribute to risk management activities, including Risk Management Plans (RMPs), REMS development, and risk minimization measure effectiveness assessments. Participate in safety governance bodies, including company safety review committees and cross‑functional benefit‑risk working groups. Monitor evolving pharmacovigilance regulations, ICH guidelines, and scientific literature relevant to drug safety in immunology, inflammation, and biologics development. Perform other duties and responsibilities as assigned. Qualifications Education: Advanced degree required; PharmD, or PhD in a biomedical or clinical discipline strongly preferred. 7+ years of pharmacovigilance or drug safety experience in the pharmaceutical or biotech industry, with demonstrated scientific and medical expertise in safety signal evaluation and benefit‑risk assessment. Deep knowledge of global PV regulatory frameworks, including FDA 21 CFR, EU GVP Modules, ICH E2A–E2F guidelines, and MedDRA coding conventions. Demonstrated experience leading or contributing to signal detection programs, including use of pharmacovigilance databases, EBGM/PRR analyses, and systematic safety literature review. Experience authoring aggregate safety reports including DSURs, PSURs/PBRERs, and Integrated Summaries of Safety (ISS) for regulatory submissions. Strong medical case review skills with experience writing and reviewing complex individual case safety narratives, including medically significant and fatal events. Proven track record of influencing without authority across organizational boundaries, driving alignment among senior stakeholders, and building consensus on complex scientific or operational priorities. Experience navigating organizational ambiguity and change; capable of defining structure, establishing priorities, and scaling functional capabilities in alignment with evolving corporate strategy. 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. Adept at facilitating productive dialogue in high‑stakes meetings, negotiations, and multi‑party collaborations; balances clarity, diplomacy, and scientific precision. Salary Range Expected annual salary range: $203,837 ‑ $212,850 USD. Benefits Medical, Dental & Vision insurance (employee premiums 100% covered by company) 20 accrued days combined time off (PTO/Sick), 12 company holidays, and winter recharge Flexible work arrangements / hybrid schedule Health Savings Account (HSA) Benefits are subject to eligibility requirements and plan terms. Additional details provided during the offer process. Equal Employment Opportunity 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. Reasonable Accommodation If you require a reasonable accommodation to participate in the application or interview process, please contact View email address on click.appcast.io to request an accommodation. We are committed to providing equal access to all candidates. Privacy 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 the Privacy Policy – Beeline Medicines. #J-18808-Ljbffr Beeline Medicines