Assoc Director, Medical Affairs
About The Position
Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. 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.
Requirements
- 10+ Years with BS/BA
- 8+ Years with MS/MA or MBA
Nice To Haves
- 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
Responsibilities
- Provide scientific and operational support for the implementation of request for proposal (RFP) programs that align with evidence-generation priorities for LEN PrEP.
- Support internal stakeholders and external investigators to develop and submit rigorous research proposals.
- Critically review research proposals submitted to RFPs, providing insight and guidance on study design, methodology and analysis plan feasibility, and strategic alignment.
- Analyze and interpret 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.
- Leverage methodologic expertise, research experience, and HIV knowledge to 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.
- Create Inclusion by demonstrating the business value of diverse and inclusive teams and embedding equity and respect into day to day people management practices.
- Develop Talent by understanding team members skills experience aspirations and potential and providing coaching feedback and development opportunities.
- Empower Teams by connecting team goals to organizational purpose removing barriers to execution and enabling cross functional collaboration.
Benefits
- Company-sponsored medical, dental, vision, and life insurance plans.
- Discretionary annual bonus
- Discretionary stock-based long-term incentives (eligibility may vary based on role)
- Paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Manager
