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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Director, U.S. Medical Affairs: Liver Strategy

Biology & BiotechConfirmed live in the last 24 hours
Full-timeFoster City, CA, USAHybrid

About the Job

Requirements

  • An advanced healthcare or scientific degree (MD, PharmD, PhD, or equivalent) is required, along with at least 8 years of experience.
  • Experience in Medical Affairs within the biopharmaceutical industry, including leadership roles in strategy and content governance.
  • Expertise in medical material development and review processes (MRC/MLR/PRC), including understanding of promotional versus non-promotional standards.
  • Ability to translate complex medical strategy into clear tactical execution and external scientific communication.
  • Experience developing scientific narratives and presentations.
  • Project and program management capabilities, including managing multiple workstreams, agencies, and timelines.
  • Experience operating in a highly matrixed, cross-functional environment and leading through influence.
  • Ability to travel domestically up to approximately 30%, including occasional weekends, as required.

Responsibilities

  • Lead development of overarching USMA Liver strategy for HCP engagement, scientific exchange, and medical education across PBC and HDV, aligned with enterprise priorities and evidence plans.
  • Translate USMA Liver strategy into executable medical tactics, including field-facing materials, scientific narratives, congress strategies, symposia content, advisory boards, and digital engagement approaches.
  • Serve as a senior Medical Affairs thought partner to Field Medical leadership, ensuring resources are field-ready, impactful, and aligned to priority HCP and KOL audiences.
  • Own end-to-end medical resource and content operations for USMA Liver, overseeing internal and external agency development, timelines, version control, and quality standards.
  • Lead U.S. Medical Review Committee governance for Liver materials, including preparation, submission, facilitating review discussions, incorporating feedback, and driving materials to approval.
  • Ensure appropriate adaptation of global medical content for U.S. use and oversee development of original U.S.-specific liver medical materials.
  • Operationalize approved resources by coordinating training, launch, distribution, and adoption across field medical, digital platforms such as CLM/MedDocs, and cross-functional teams.
  • Maintain lifecycle management of liver medical assets, including renewals, expirations, proactive updates, and inventory of live materials.
  • Lead HDV tactical planning and execution, including Annual Encore planning, congress deliverables, and ad hoc initiatives based on evolving priorities.
  • Shape external scientific narrative by translating emerging clinical, real-world, and guideline data into clear, balanced, and compliant scientific communications.
  • Partner cross-functionally with Legal, Regulatory, Commercial, HEOR, GMA, Clinical, Training, and Operations to ensure aligned, integrated, and compliant execution.
  • Drive operational excellence, clear prioritization, and efficient use of resources across projects, vendors, and assigned budget areas.
  • Contribute to digital and innovation strategy for USMA Liver, including evaluating and deploying digital and AI-enabled solutions to enhance insight generation and medical education.
  • Uphold Gilead core values and ensure all activities comply with applicable laws, regulations, and internal policies.
  • Create inclusion by modeling inclusion and embedding the value of diversity in how teams are managed.
  • Develop talent by understanding employees’ skills, experience, aspirations, and potential, coaching them on performance and future potential, and ensuring they receive feedback and insight to grow and develop.
  • Empower teams by aligning goals, purpose, and organizational objectives, holding teams accountable, removing barriers, and connecting teams to the broader ecosystem.

Desired Qualifications

  • Experience with digital medical content and innovation approaches to HCP education.
  • Strong background in liver disease, including PBC, viral hepatitis, or related areas.
  • 8–12+ years of relevant experience.

About the Company

Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Gilead Sciences is a biopharmaceutical company that discovers, develops and sells medicines for HIV, viral hepatitis and other liver diseases, cancer and inflammatory conditions. Its HIV business covers both treatment, led by the once-daily pill Biktarvy, and prevention, including Descovy and Yeztugo, a lenacapavir injection given twice a year. In cancer, its Kite unit makes CAR T-cell therapies from patients' own immune cells, and Trodelvy is an antibody-drug conjugate for breast cancer. Gilead earns revenue by selling its drugs to wholesalers, specialty pharmacies, hospitals and governments worldwide after regulatory approval. The company was founded in 1987 and is headquartered in Foster City, California.

Company size
10,001+
Company stage
IPO
Headquarters
Foster City, CA
Founded
1987

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