Director, Medical Affairs Research – Oncology

Director, Medical Affairs Research

The Director, Medical Affairs Research – Oncology, you will serve as a senior research lead within Oncology Medical Affairs, responsible for defining and executing medical affairs led evidence generation across the oncology portfolio. This role will be used to hire multiple Directors with complementary methodological expertise.

Directors in this role must bring deep expertise in one or more of the following methodological areas: interventional (Phase 4 and collaborative) research, observational / real‑world evidence research, and implementation science. While each Director is expected to anchor in at least one primary area of expertise, all will collaborate closely to deliver integrated, fit‑for‑purpose evidence aligned to Integrated Evidence Plans (IEPs).

Essential Duties & Job Functions

• Lead Oncology Medical Affairs Research strategy aligned to Integrated Evidence Plans across assets and disease areas
• Provide scientific leadership for late‑phase oncology research, selecting and applying appropriate methodologies based on evidence gaps
• Serve as Medical Affairs Study Lead (MASL) for Gilead‑sponsored and collaborative research studies
• Define research questions and guide protocol development for interventional, observational, and/or implementation science studies
• Oversee a portfolio of Oncology MAR studies, ensuring scientific rigor, operational feasibility, governance, and compliance
• Influence cross‑functional partners across Development, HEOR, Commercial, Safety, and external stakeholders
• Build and sustain external scientific partnerships including academic investigators, cooperative groups, data partners, and health systems
• Translate study findings into scientific communications such as abstracts, manuscripts, and presentations
• Provide mentorship and scientific leadership within Oncology Medical Affairs to strengthen research capability
• Ensure adherence to regulatory, legal, and business conduct standards governing Medical Affairs research

Key Capabilities & Methodological Expertise

Candidates must demonstrate deep expertise in one or more of the following areas. Expertise in multiple areas is strongly preferred.

• Interventional Research: Expertise in Phase 4 interventional trial design and conduct, including protocol development, feasibility assessment, execution oversight, and collaboration with academic and cooperative research groups.
• Observational / Real‑World Evidence Research: Expertise in observational study design and analysis, including use of real‑world data sources such as claims, EHRs, registries, and linked datasets, with strong understanding of epidemiologic and methodological rigor.
• Implementation Science Research: Expertise in implementation science frameworks and mixed‑methods research, focused on translating evidence into real‑world oncology practice, addressing care gaps, and driving adoption and sustainability.

Knowledge & Skills

• Demonstrated scientific credibility and thought leadership in oncology research
• Experience serving as major contributing author on manuscripts, abstracts, or scientific congress submissions.
• Strong strategic thinking with ability to translate complex evidence gaps into actionable research plans
• Proven ability to influence and collaborate across complex, matrixed organizations
• Excellent interpersonal, written, and verbal communication skills
• Ability to operate effectively in a global environment
• High standards of integrity, accountability, and commitment to compliant scientific exchange

Education & Experience

• Advanced scientific or medical degree (e.g., PhD, PharmD, MD, MPH) required.
• Demonstrated history of scientific publications and/or authorship in peer‑reviewed journals within the candidate’s primary area of methodological expertise (interventional clinical research, observational / real‑world evidence, and/or implementation science).
• Typically, 10+ years of experience in oncology research, medical affairs, or related pharmaceutical or academic settings.
• Significant experience leading late‑phase research, including Phase 4, collaborative, and Medical Affairs‑led studies.
• Strong understanding of regulatory, ethical, and compliance requirements governing Medical Affairs research activities.

Basic Qualifications

• Bachelor's Degree and Twelve Years’ Experience
• OR
• Masters' Degree and Ten Years’ Experience
• OR
• PhD, PharmD, MD, MPH and Eight Years’ Experience

People Leader Accountabilities:

• Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
• Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
• Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

The salary range for this position is: $243,100.00 - $314,600.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock‑based long‑term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing

• Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States:

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 regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

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