Assoc Director, Medical Affairs
Gilead Sciences
Summary
We are seeking an Associate Director to join our Phase 4 HIV Prevention Medical Affairs Research team. This role will support evidence-generation priorities for LEN PrEP, including Phase 4 Gilead-sponsored, collaborative, and investigator-initiated research; proposal development and review; and translation of research findings into abstracts, manuscripts, and scientific presentations. The ideal candidate brings strong methodological expertise in observational, clinical, and/or implementation research, a solid understanding of HIV prevention and treatment, and the ability to work effectively in a fast-paced, cross-functional environment with internal and external stakeholders. Additional experience with data analysis and statistical software is preferred but not required. This position is based in Foster City, California & does not provide relocation assistance.
Job description
Specific Job Responsibilities
- Implementation of request for proposal (RFP) programs that align with evidence-generation priorities for LEN PrEP
- Support for internal stakeholders and external investigators to develop and submit rigorous research proposals
- Critical review of research proposals submitted to RFPs, providing insight and guidance on study design, methodology and analysis plan feasibility, and strategic alignment
- Analysis and interpretation of data from the PROPEL study, a Gilead-sponsored, Phase 4, Hybrid Effectiveness-Implementation Study of LEN PrEP implementation in the U.S.
- Contribute to cross-functional HIV evidence-generation efforts, including coordination of data generation plans and management of study metric trackers
- Work with Gilead team members and external investigators, to design, develop, and serve as Medical Affairs lead for collaborative studies
- Provide high-quality technical and methodological input to cross-functional teams to effectively use research learnings to optimize prevention practice and improve health outcomes
- Lead, coordinate, and track the development of communications (e.g., abstracts, manuscripts, scientific forum presentations, slide decks) to build the peer-reviewed published evidence base from Phase 4 HIV prevention research
- Provide support at advisory boards, conferences, and other external meetings.
- Adhere to all applicable pharmaceutical codes, Office of Inspector General (OIG) guidelines, and Gilead policies
- Exhibit Gilead’s core values: integrity, teamwork, accountability, excellence, and inclusion
Basic Qualifications
- 10+ Years with BS/BA OR 8+ Years with MS/MA or MBA
Preferred Qualifications
- Advanced degree (Ph.D., MD, PharmD) in a scientific, medical, or public health discipline (e.g., epidemiology, implementation science, health policy, data science)
- 5-8 years’ experience conducting HIV clinical, observational, and/or implementation research with specialized training in research methods (e.g., epidemiology, biostatistics, implementation science, health economics). Candidates with fewer years of research experience who demonstrate strong, directly relevant research capabilities and potential for success in the role are encouraged to apply.
- Experience and success with developing research abstracts and peer reviewed manuscripts for publication.
- Pharma/biotech industry experience
- Proficiency with data analysis and use of statistical software (e.g., R, STATA, SAS)
- Strong attention to detail, with the ability to understand and interpret quantitative data, synthesize scientific literature, and critically review research study protocols
- Excellent written and verbal communication skills, with the ability to translate complex scientific concepts into clear and concise language for diverse audiences in varying formats.
- Strong organizational skills and ability to work independently in a cross-functional environment.
- Proficiency in Microsoft Office
Requirements
- 10+ Years with BS/BA OR 8+ Years with MS/MA or MBA
- Advanced degree (Ph.D., MD, PharmD) in a scientific, medical, or public health discipline
- 5-8 years’ experience conducting HIV clinical, observational, and/or implementation research
- Experience and success with developing research abstracts and peer reviewed manuscripts for publication
- Pharma/biotech industry experience
- Proficiency with data analysis and use of statistical software (e.g., R, STATA, SAS)
- Strong attention to detail, with the ability to understand and interpret quantitative data, synthesize scientific literature, and critically review research study protocols
- Excellent written and verbal communication skills
- Strong organizational skills and ability to work independently in a cross-functional environment
- Proficiency in Microsoft Office
Benefits
- Medical, Dental & Vision
- Life Insurance
- Paid Time Off
- Annual Bonus
- Stock-based Long-term Incentives
Company overview
Gilead Sciences, Inc. is a leading American biopharmaceutical company headquartered in Foster City, California, that specializes in researching, developing, and commercializing innovative medicines for life-threatening diseases. Founded in 1987, Gilead has grown into a global healthcare leader with approximately 17,600 employees worldwide. The company's primary therapeutic focus areas include HIV/AIDS, viral hepatitis (hepatitis B and C), oncology, inflammation, and respiratory diseases. Gilead is renowned for its groundbreaking antiviral therapies, including Sovaldi and Harvoni for hepatitis C, and its comprehensive portfolio of HIV treatments such as Truvada, Atripla, and Biktarvy. The company also developed Veklury (remdesivir) for COVID-19 treatment. Gilead operates as a publicly traded company on the NASDAQ (GILD) and is a component of both the Nasdaq-100 and S&P 100 indices. Through strategic acquisitions like Kite Pharma and Immunomedics, Gilead has expanded into cell therapy and oncology, demonstrating its commitment to advancing medical science and improving patient outcomes globally.