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 HIV, viral hepatitis, COVID-19, oncology, and inflammatory diseases. From curing hepatitis C to revolutionizing HIV treatment and prevention, Gilead's innovative therapies have transformed patient lives globally. Headquartered in Foster City, California, the company fosters a culture of collaboration, determination, and bold ambition, empowering employees to drive life-changing scientific advancements.

Role Overview

As Director, RWE Virology Safety Epidemiology at Gilead Sciences, you will lead real-world evidence (RWE) initiatives within the Clinical Data Sciences group. Reporting to the Senior Director, RWE Safety Therapeutic Area Lead-Virology, this role focuses on executing safety epidemiology studies across the virology product lifecycle, including pediatrics, post-authorization studies (PAS), and pharmacoepidemiology activities. Based in Foster City, California, Cambridge, UK, or Stockley Park, UK, you will partner with cross-functional teams to ensure regulatory compliance and high-quality RWE supporting Gilead's virology portfolio, which tackles major public health challenges like HIV and viral hepatitis.

Key Responsibilities

In this pivotal leadership position, your responsibilities include developing, executing, and communicating RWE safety and non-experimental studies for virology products and pipeline indications. You will act as the key subject matter expert for post-marketing commitments (PMCs) and other safety activities, advocating for optimal resources and methods to meet internal and external stakeholder needs, such as regulators. Collaboration with RWE Virology Product teams and global stakeholders is essential to deliver timely, high-quality outcomes. Success demands expertise in observational research within a matrix organization, ensuring excellence in safety epidemiology from drug development through commercialization.

Core Duties

• Oversee RWE safety studies, including mandatory and voluntary PAS.
• Provide functional expertise on RWE methods at global, regional, and therapeutic area levels.
• Manage cross-functional efforts for virology safety pharmacoepidemiology.
• Ensure application of contemporary analytical methods using real-world data (RWD).

Qualifications & Requirements

Candidates must possess a strong track record in designing and conducting epidemiologic studies, with direct expertise in RWE and RWD applications across drug development phases, including pediatrics and post-authorization. An advanced degree in epidemiology, public health, pharmacoepidemiology, or a related field is required, alongside proven ability to manage resources in a matrix environment. Experience with virology products, regulatory interactions, and global study execution is critical. Proficiency in analytical tools and methods for observational research will set you apart in this role at Gilead Sciences.

Essential Skills

• Expertise in pharmacoepidemiology and safety studies.
• Leadership in cross-functional teams.
• Knowledge of regulatory requirements for PMCs and PAS.
• Strong communication for stakeholder engagement.

Benefits & Perks

Gilead Sciences offers a comprehensive benefits package designed to support your professional and personal well-being. Enjoy competitive compensation, health insurance, retirement plans, and generous paid time off. Employees benefit from onsite fitness centers, flexible work arrangements, and family-friendly policies. As a people leader, you'll access leadership development programs to foster an inclusive culture where every team member thrives.

Career Growth

At Gilead, career advancement is a priority. This Director role positions you for senior leadership in RWE and Clinical Data Sciences, with opportunities to influence Gilead's virology strategy and beyond. Mentoring programs, internal mobility, and continuous learning ensure you evolve alongside groundbreaking innovations in HIV, oncology, and inflammatory diseases. Gilead invests in your growth to help you make a lasting impact on global health.

Why Join Gilead

Joining Gilead means contributing to bold ambitions against the world's biggest health challenges. Work on therapies that cure diseases like hepatitis C, advance HIV care, and pioneer oncology treatments. Our matrix organization values collaboration, empowering you to lead transformative RWE initiatives. With a commitment to diversity, inclusion, and employee empowerment, Gilead provides the platform to fulfill your aspirations while creating possible together.

Role FAQs

What is the reporting structure?

You report to the Senior Director, RWE Safety Therapeutic Area Lead-Virology, within a matrix organization.

Are there relocation opportunities?

Positions are available in Foster City, CA; Cambridge, UK; or Stockley Park, UK, with potential support for high-caliber candidates.

What experience is most valued?

Proven expertise in RWE safety epidemiology for virology, including post-marketing studies and regulatory interactions.

How does this role impact Gilead's mission?

You ensure robust safety data supports life-changing therapies for HIV, viral hepatitis, and beyond, aiding global access.

This role offers a unique chance to leverage your epidemiology expertise at a world-class biopharma leader. Apply to shape the future of virology safety research at Gilead Sciences.