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 therapies that address some of the world's most pressing health challenges, including HIV, viral hepatitis, COVID-19, and cancer. The company's relentless pursuit of innovation has resulted in a cure for hepatitis C, revolutionary advancements in HIV treatment and prevention, and significant progress in therapies for viral, inflammatory diseases, and certain cancers. Headquartered in Foster City, California, Gilead employs thousands of passionate professionals united by a mission to improve lives and ensure global access to life-changing medicines.

Gilead's work in HIV has transformed patient outcomes worldwide, while its oncology portfolio pushes the boundaries of cancer care. In inflammatory diseases, Gilead is developing cutting-edge treatments for conditions like rheumatoid arthritis and inflammatory bowel disease. This Director, Clinical Development (MD) role positions you at the heart of these efforts, contributing to bold ambitions in immunology clinical development.

Role Overview

As Director, Clinical Development (MD) at Gilead Sciences in Foster City, California, you will lead multiple components of clinical trial programs in immunology. This site-based role at Gilead's global headquarters offers a hybrid environment, allowing work from home on Mondays and Fridays. You will act as a key physician responsible for projects, overseeing protocol preparation, data analysis, regulatory documentation, and scientific presentations. This position demands a blend of clinical expertise, strategic leadership, and adaptability to drive clinical development deliverables in a fast-paced biopharma setting.

Join a team that's confronting public health challenges head-on, from advancing HIV therapies to innovating in oncology and inflammatory diseases. Your contributions will directly impact patients and shape the future of medicine.

Key Responsibilities

In this pivotal role, you will:

• Provide input into or lead the development of the Target Product Profile and Clinical Development Plan for assigned molecules/products.
• Offer scientific and clinical guidance to cross-functional teams to meet project deliverables and timelines.
• Lead clinical trial protocol design, clinical study reports, and responses to health authority inquiries.
• Conduct ongoing medical monitoring for clinical trials, including eligibility assessment, toxicity management, and drug safety surveillance.
• Manage clinical development components in regulatory documents, investigator brochures, and development plans.
• Coordinate data collection, analysis, listings, summary tables, study results, and scientific presentations.
• Present at scientific conferences and clinical study investigator meetings.
• Adhere to Good Clinical Practice standards, regulatory requirements, and Gilead SOPs.

Qualifications & Requirements

Gilead seeks candidates who bring unique contributions to serve patients. Minimum qualifications include:

• MD or equivalent with 4+ years of clinical, scientific, or drug development experience in biopharma, healthcare, consulting, academia, or related fields.
• Preferred experience in Phase 1 and 2 clinical trials.
• Board certification in rheumatology, dermatology, gastroenterology, or allergy and immunology, with familiarity in systemic autoimmune diseases.
• Biopharma industry experience preferred.
• Proven track record leading small cross-functional project teams in clinical research or development.
• Experience in study concept/protocol design, regulatory filings, medical monitoring, clinical publications, and presentations.
• Demonstrated effectiveness in matrix management of clinical project deliverables.

Key attributes: fast learner, flexible and adaptable, ability to shift between projects seamlessly. As a people leader, you will create inclusion, model diversity, and embed these values in team management.

Knowledge & Other Requirements

Strong knowledge of clinical development processes, regulatory landscapes, and industry standards is essential. Your ability to provide expertise across projects will be critical in Gilead's dynamic environment.

Benefits & Perks

Gilead Sciences offers a comprehensive benefits package designed to support your well-being and professional growth:

• Hybrid work model with flexibility for remote work on Mondays and Fridays from the Foster City headquarters.
• Competitive salary estimated at $350,000 - $450,000 annually, based on biopharma sector rates for similar roles in California.
• Comprehensive health, dental, and vision insurance.
• 401(k) matching, stock purchase plans, and performance bonuses.
• Generous paid time off, parental leave, and wellness programs.
• Professional development opportunities, including leadership training and tuition reimbursement.

These perks reflect Gilead's commitment to employee inclusion, development, and empowerment.

Career Growth

At Gilead, every employee is empowered to fulfill their aspirations. As a Director, you will have access to mentorship from top leaders, cross-functional exposure, and opportunities to lead high-impact projects. Gilead's focus on people leadership fosters an environment where diverse teams drive innovation. Advance your career in clinical development, potentially moving into VP roles or broader R&D leadership, while contributing to therapies in HIV, oncology, and inflammatory diseases.

Why Join Gilead

Join Gilead to be part of a mission-driven organization tackling the world's biggest health challenges. Work alongside ambitious professionals on groundbreaking science that improves lives globally. Gilead's culture emphasizes collaboration, determination, and inclusion, making it an ideal place for MDs passionate about clinical development in immunology. In Foster City, enjoy California's vibrant innovation hub, proximity to top talent, and a supportive hybrid work culture. Make a direct impact—together, create possible.

Role FAQs

Is this role hybrid or fully on-site?

This is a site-based role at Foster City, CA, with a hybrid environment allowing work from home on Mondays and Fridays.

What experience level is required?

MD with 4+ years in clinical/drug development; Phase 1/2 trial experience and board certification in relevant fields preferred.

Does Gilead sponsor visas?

Gilead supports diverse talent; visa sponsorship may be available based on qualifications—check the application for details.

What diseases does this role focus on?

Primarily immunology clinical development, aligning with Gilead's work in inflammatory diseases, alongside HIV and oncology advancements.

How does Gilead support leadership development?

Through people leader training, inclusion initiatives, and opportunities to lead cross-functional teams on high-stakes projects.