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Base pay range
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Job Title: Medical Affairs Associate Manager
Location: Foster City, CA 94404
Duration: 04+ months contract
Position Summary
- Reports to the Sr. Director of Viral Hepatitis, Global Medical Affairs.
- Global role within the Liver, Inflammation, Fibrosis and Established Products (LIFE) Medical Affairs organization.
- Responsible for developing and executing global strategies for products in the LIVE franchise.
- Collaborates across viral hepatitis and potentially other LIVE therapeutic areas based on business needs.
Key Responsibilities
- Develop and execute global strategic and tactical medical affairs activities for the LIVE franchise.
- Collaborate with internal and external stakeholders, including Medical Affairs, Scientific Publications, Marketing, Clinical Research, Value and Market Access, Public Affairs, Legal, and other functions.
- Serve as subject matter expert on LIVE products, Client pipeline, and competitive landscape.
- Prepare materials for internal/external meetings, advisory boards, and training programs.
- Support data generation through review and management of investigator-sponsored research, Phase 3b, and Phase 4 studies.
- Review abstracts, manuscripts, and scientific communications from Phase IV programs.
- Participate on Global Publications and Scientific Message Platform committees.
- Provide medical/scientific coverage at key meetings and conferences.
- Manage promotional material review for GRC and MRC.
- Track budgets, purchase orders, and invoicing for the viral hepatitis franchise.
- Perform other duties as assigned to support LIVE Medical Affairs.
- Strong written, verbal, interpersonal, relationship-building, and negotiation skills.
- Excellent organizational skills with ability to manage multiple projects and meet deadlines.
- Strong analytical and problem-solving abilities; ability to interpret complex scientific data.
- Proven teamwork skills with attention to detail in fast-paced environments.
- Experience in public health or internal medicine (general or subspecialty) preferred.
- Demonstrated ability to develop abstracts, manuscripts, posters, and scientific presentations.
- Familiarity with regulatory and legal requirements (FDA, ICH, GCP) for clinical trials and medical affairs.
- Ability to work independently with minimal supervision.
- Willingness to work across international time zones and travel domestically/internationally, including occasional weekends.
Qualifications
- Preferred: M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD.
- Prior experience in hepatology, infectious diseases, virology, or clinical virology desirable.
- Experience in Medical Affairs and/or Clinical Research, including Phase IIIb/IV studies, clinical trials management, and medical monitoring preferred.
Seniority level
Seniority level
Associate
Employment type
Employment type
Contract
Job function
Job function
ScienceIndustries
Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research
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