Senior Director, Medical Affairs Research LIVE

Overview

Senior Director, Phase 4 Research LIVE – to join the Global Medical Affairs team at Gilead in Foster City, CA. The role leads execution of the Medical Affairs-led LIVE research strategy, aligns research strategy with clinical development plans and asset strategy, serves as Gilead study lead for key interventional Phase 4 studies in LIVE, and helps oversee Gilead's LIVE investigator sponsored research (ISR) program. The ideal candidate is an established leader in clinical and/or implementation research in virology or inflammation with a strong publication record and deep understanding of LIVE therapeutic areas. Educational and other Requirements and responsibilities we keep in this section reflect the original job’s emphasis on leadership in research strategy and execution for Phase 4 LIVE programs. Responsibilities

Develop and lead execution of Gilead's Medical Affairs-led LIVE research strategy Lead and provide scientific and methodological expertise for Phase 4 interventional and implementation studies, in particular in support of new product launches for future assets Oversee Gilead's investigator sponsored research program in LIVE, including determining ISR funding priorities in line with Phase 4 integrated evidence plans (IEPs), oversight of RFP development and execution, and working with Gilead's clinical operations team to manage the ISR portfolio Lead and support the development of research communications (e.g., abstracts, manuscripts, scientific forum presentations, slide decks) to build the peer reviewed published evidence base from Phase 4 research Ensure alignment of research strategy with the clinical development plans and overarching asset strategy Lead and support Gilead LIVE cross-functional data generation efforts Lead or serve as core member of IEP working groups in LIVE Lead/co-Lead or participate in IEP execution teams (ETs) consolidate and coordinate data generation efforts cross-functionally to ensure IEP alignment and strategic data gap fulfillment of proposed and ongoing research efforts Socialize data generation outputs to cross-functional senior and executive leadership Provide strategic leadership and support of the MA Phase 4 research program proposal review process Work with the Research Committee (RC) chair and team lead to ensure smooth execution of ISR and Gilead Sponsored proposal reviews Lead the development of asset-specific RFPs to ensure high-quality, strategically aligned submissions from expert external investigators Serve as standing member of the LIVE treatment global and investigator sponsored research committees (GRC/IRC): provide insight and guidance on study design, methodology and analysis plan feasibility and strategic alignment for study proposals Work with local medical affairs and other Phase 4 research teams in real world research and HEOR to ensure strategically aligned and high-quality local sponsored study proposals Provide expert reviews of study protocols for functional (GMA) and cross-functional protocol review boards Collaborate with the RC therapeutic area and process leads to ensure tracking of Phase 4 studies and impact measurement Collaborate with the publications team in publications planning for key conferences and high-quality journals Lead and provide expertise 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 Educational and other Requirements

Medical degree and/or advanced degree in a scientific, medical or public health discipline (Ph.D., MD, PharmD) 10 years' plus experience leading and conducting interventional (clinical and/or implementation) research in virology with specialized training in research methods Proven publication track-record for research abstracts presented at major conferences and high-impact peer reviewed journals Preferred Qualifications

Research and/or clinical experience in TAs covered under LIVE Community-based, PRO, qualitative and/or mixed methods research experience Pharma / Biotech Industry experience Proficiency in statistical and qualitative data analysis software packages, Microsoft Office suite and reference management software Excellent written and verbal communication skills, with the ability to translate complex scientific concepts into clear and concise language for diverse audiences Strong attention to detail and ability to critically analyze data and scientific literature Strong organizational skills and ability to work independently Compensation

The salary range for this position is: Bay Area: $281,010.00 - $363,660.00 Other US Locations: $255,425.00 - $330,550.00 Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package. Equal Opportunity and Notice

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, disability, or other protected characteristics. Reasonable accommodations are available on request. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Job Requisition ID R0046186

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