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Medical Director, Safety and Pharmacovigilance (Office OR Remote)
Arcus BiosciencesUnited StatesRemotefull_timeVerifiedPosted 29 Apr 2025
💰 $320,000/yr($280,000/yr – $320,000/yr)
About the role
The Medical Director, Safety and Pharmacovigilance will provide medical expertise across the growing Arcus clinical portfolio by supporting a variety of core medical activities including the management of safety signal, risk management, and benefit-risk strategies for the assets as well as support medical reviewer on individual case safety reports (ICSRs). This individual must effectively collaborate cross-functionally at all levels of the organization as well as with external Regulatory Authorities. This leader will report into the Executive. Medical Director for Patient Safety and Pharmacovigilance. Responsibilities:
- Develop, contribute to, and oversee the execution of the signal detection strategy for the Arcus portfolio.
- Coordinate cross-functional Safety Review Teams and Chairs Safety Management Committees.
- Preparation and review of periodic aggregate reports (IND Annual Reports, Development Safety Update Reports (DSUR), Periodic Benefit Risk Evaluation Report (PBRER), EU renewal, etc.)
- Review, contribute, and author as appropriate, relevant sections of the clinical trial protocols, the Investigator’s Brochure (IB), Company Core Data Sheet (CCDS), informed consent form (ICF) and other study specific documents to ensure alignment with the asset benefit-risk profiles.
- Leads the effort to create developmental risk management plans by seeking input from cross-functional stakeholders.
- Provides strategic medical input into Regulatory Authority safety assessments and requests for information.
- Prepare and review relevant sections of the Regulatory Authority filing and submission documents for NDs, NDA/BLA/MAAs, etc.
- Participate in and provide input for internal monitoring committees, iDMCs/DSMBs, as applicable.
- Contribute to scientific publications (abstracts, posters, papers) for scientific meetings and/or journals.
- Contribute, as appropriate, to the medical safety evaluation of projects for new business development opportunities (e.g., due diligence evaluations).
- Education: Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) degree required. Academic or hospital setting oncology experience preferred.
- 3+ years’ relevant Safety experience required. Experience working in oncology including NDA/BLA submission activities are preferred but not required.
- Demonstrated ability to create, evaluate, and maintain effective business processes and implement procedures, systems, and tools to maximize resources within the Safety department.
- Demonstrated ability to work effectively in a dynamic, complex, cross-functional, and fast-paced team environment.
- Excellent interpersonal, communication, analytical, and organizational skills.
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