Sr Director, Medical Affairs

Role Summary

Senior Director of Medical Affairs Research in the Liver, Inflammation, Respiratory Viruses, and Established Products (LIVE) group. Lead a team of scientists and project managers to drive the development and execution of phase 4 research strategy, align research with clinical development plans and asset strategy, and oversee LIVE investigator sponsored research programs. Based in Foster City.

Responsibilities

• Provide leadership and oversight of a team of experienced scientists and program managers. Foster their scientific development and career evolution.
• Lead and provide scientific and methodological expertise for Phase 4 interventional, observational and implementation studies.
• Develop and lead execution of Gilead’s Medical Affairs-led (Phase 4) LIVE research strategy from concept through dissemination and publication; ensure alignment with integrated evidence plans, clinical development plans, and asset strategy; oversee global, regional, and local processes.
• Lead and provide expertise at advisory boards, conferences and other external meetings.
• Adhere to pharmaceutical codes, OIG guidelines, and Gilead policies.
• Demonstrate core values: integrity, teamwork, accountability, excellence, and inclusion.

Qualifications

• Required: Medical degree and/or advanced degree in a scientific, medical or public health discipline (Ph.D., MD, PharmD).
• Required: 10+ years’ experience leading and conducting interventional (clinical and/or implementation) research in virology with specialized training in research methods.
• Required: Proven publication track record for research abstracts presented at major conferences and high-impact peer-reviewed journals.
• Required: Experienced manager, including direct reports and cross-functional teams engaged in research studies and related projects.
• Preferred: Research and/or clinical experience in LIVE therapeutic areas.
• Preferred: Community-based, PRO, qualitative and/or mixed methods research experience.
• Preferred: Pharma/Biotech industry experience.
• Preferred: Proficiency in statistical and qualitative data analysis software, Microsoft Office, and reference management software.
• Preferred: Excellent written and verbal communication skills with ability to translate complex scientific concepts for diverse audiences.
• Preferred: Strong attention to detail, ability to critically analyze data and literature, and strong organizational skills with ability to work independently.

Education

• Medical degree and/or advanced degree in a scientific, medical or public health discipline (Ph.D., MD, PharmD).

Skills

• Leadership of scientific teams and program management
• Phase 4 interventional, observational, and implementation study design and execution
• Strategic alignment of research plans with clinical development and asset strategy
• External engagement at advisory boards, conferences, and meetings
• Strong scientific writing and communication abilities