About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered breakthroughs in treating some of the world's most devastating diseases, including HIV, viral hepatitis, COVID-19, and cancer. The company's innovative therapies have delivered a cure for hepatitis C, revolutionary advancements in HIV treatment and prevention, and significant progress in oncology and inflammatory diseases. Headquartered in the United States, Gilead operates globally, ensuring access to life-changing medicines while fostering collaboration, determination, and scientific excellence. With a bold mission to confront major public health challenges, Gilead empowers its employees to drive scientific innovations that improve patient lives for generations.

Role Overview

The Director, Medical Affairs Framework at Gilead Sciences in Parsippany, New Jersey, plays a pivotal role in upholding the highest standards of ethics, transparency, and compliance within US Medical Affairs (USMA). This leadership position involves designing and implementing robust frameworks for medical content, scientific exchange, evidence generation, and external engagements. Reporting into key medical leadership, the Director ensures all USMA activities—from publications and investigator-initiated research to advisory boards and medical information—adhere to internal policies, FDA guidelines, PhRMA Code, and OIG requirements. This is an opportunity for a seasoned professional to shape medical governance, partner with cross-functional teams, and contribute to Gilead's patient-centric mission in HIV, oncology, and inflammatory diseases.

Key Responsibilities

In this critical role, the Director will:

• Develop, lead, and continuously improve the U.S. Medical Affairs framework to support compliant medical operations and decision-making.
• Drive comprehensive medical affairs framework and ethical training programs, ensuring ongoing training for USMA and US Affiliate teams.
• Collaborate with Global Learning and Development for effective employee onboarding into the USMA framework.
• Provide medical contributions to the Promotional Review Committee (PRC) and Medical Review Committee (MRC), managing escalations for timely, compliant reviews.
• Oversight governance for U.S. medical field activities, including MSL engagements, scientific exchange, advisory boards, and investigator-sponsored studies.
• Partner closely with U.S. Commercial, Regulatory, Legal, and Compliance teams to align business objectives with framework standards.
• Monitor emerging global and U.S. regulatory trends, conduct risk assessments, and implement control measures.
• Develop metrics and dashboards to track key performance indicators for the Medical Affairs framework.
• Support audits, inspections, and maintain audit-ready documentation.

Qualifications & Requirements

To succeed in this role, candidates should possess:

• A BS/BA degree in a scientific, medical, or related field; advanced degree (MD, PharmD, PhD) strongly preferred.
• 10+ years of experience in US Medical Affairs, pharmaceutical compliance, or regulatory roles within biopharma.
• Proven expertise in FDA promotional guidelines, PhRMA Code, OIG compliance, and industry standards.
• Strong leadership skills with experience developing training programs and managing cross-functional partnerships.
• Excellent communication and analytical abilities to handle complex medical governance and risk management.
• Demonstrated track record in scientific integrity, patient safety, and ethical medical operations.

Up-to-date knowledge of clinical, ethical, and compliance trends is essential, along with the ability to thrive in a dynamic, regulated environment.

Benefits & Perks

Gilead Sciences offers an exceptional total rewards package designed to support employee well-being and professional success:

• Competitive base salary with annual incentives and long-term equity awards.
• Comprehensive medical, dental, vision coverage, and life insurance options.
• 401(k) plan with generous company matching contributions.
• Flexible paid time off, including vacation, sick leave, and paid holidays.
• Wellness programs, onsite fitness facilities, and mental health resources.
• Tuition reimbursement and professional development opportunities.

Career Growth

At Gilead, career advancement is a priority. As a People Leader, you'll drive cultural evolution, employee inclusion, and empowerment. This Director role provides exposure to senior leadership, global medical strategies, and high-impact projects in HIV, oncology, and inflammatory diseases. Gilead invests in leadership training, mentorship, and internal mobility, enabling ambitious professionals to achieve bold aspirations and make direct impacts on global health challenges.

Why Join Gilead

Joining Gilead means becoming part of a team united in relentless pursuit of scientific innovation. Contribute to therapies transforming lives in HIV treatment, oncology breakthroughs, and inflammatory disease management. Work in a collaborative environment in Parsippany, New Jersey, with access to cutting-edge resources and a culture valuing ethics, integrity, and patient-centricity. Gilead's commitment to bold ambitions ensures you'll thrive while advancing your career in biopharma.

Role FAQs

What is the work environment like?

This is a hybrid role in Parsippany, NJ, blending office collaboration with flexibility, emphasizing ethical leadership and compliance.

Is travel required?

Occasional travel for meetings, audits, or engagements may be needed.

What makes this role unique at Gilead?

Direct influence on medical frameworks supporting groundbreaking work in HIV, oncology, and inflammatory diseases.

How does Gilead support professional development?

Through targeted training, leadership programs, and partnerships with Global Learning and Development.

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