About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company headquartered in Foster City, California, with a proven track record of over 35 years in developing groundbreaking therapies. Renowned for its work in HIV, viral hepatitis, COVID-19, and cancer, Gilead has transformed patient lives worldwide through innovative medicines. The company operates in more than 35 countries, focusing on scientific invention to address life-threatening diseases. Gilead's portfolio includes pioneering HIV treatments like Biktarvy and oncology advancements through its Kite Pharma subsidiary. Additionally, Gilead is expanding into inflammatory diseases, delivering targeted therapies that improve outcomes for patients facing complex health challenges. With a mission to create a healthier world for all, Gilead fosters a collaborative environment where ambitious professionals drive real impact.

Role Overview

The Associate Clinical Pharmacology Director role at Gilead Sciences in Foster City, California, is a pivotal leadership position within drug development teams. This expert will spearhead clinical pharmacology strategies for products targeting HIV, oncology, and inflammatory diseases. Based in the state-of-the-art Foster City office—or potentially Parsippany, NJ—this full-time position demands a blend of scientific acumen, strategic planning, and cross-functional collaboration. As a key contributor to clinical development plans, you will author pharmacology strategies, lead complex studies, and interface with regulatory bodies like the FDA and EMA. This role offers the chance to influence life-changing therapies while thriving in Gilead's innovative culture.

Strategic Impact in Biopharma

In this director-level position, you'll provide critical input into product development, ensuring clinical pharmacology aligns with Gilead's bold ambitions in HIV and oncology. Your work will directly support regulatory filings and global access to therapies, embodying Gilead's commitment to scientific excellence.

Key Responsibilities

As Associate Clinical Pharmacology Director, your responsibilities span study leadership, analysis, and stakeholder engagement. Core duties include:

• Routinely providing strategic input into product development and clinical plans for assigned HIV, oncology, or inflammatory disease projects.
• Authoring comprehensive clinical pharmacology plans for one or more products.
• Leading the design, conduct, and monitoring of increasingly complex clinical pharmacology studies, managing cross-functional teams.
• Designing protocols, data analysis, modeling, and simulation plans with PK-PD focus.
• Conducting analyses, interpreting results, and authoring documents for clinical and regulatory submissions.
• Representing clinical pharmacology in regulatory interactions and business development activities.
• Managing timelines, resources, and resolving issues while adhering to GCP, FDA/EMA regulations, and Gilead SOPs.

Cross-Functional Leadership

You'll direct internal and external partners, present milestones to stakeholders, and anticipate trial challenges with innovative solutions, ensuring seamless execution.

Qualifications & Requirements

Gilead seeks candidates with strong scientific credentials and proven leadership. Basic qualifications include:

• Doctorate and 5+ years of relevant experience; OR Master’s and 8+ years; OR Bachelor’s and 10+ years.

Preferred qualifications elevate your candidacy:

• PhD or PharmD in pharmaceutical sciences, pharmacology, or related field.
• Excellent communication skills to convey complex technical information.
• Proficiency in pharmacokinetic software like WinNonlin.
• Experience leading cross-functional teams, protocol design, and regulatory filings.
• Knowledge of FDA, EMA, ICH guidelines, and GCP.
• Demonstrated adaptability, fast learning, and flexibility across projects.

Why These Matter

These qualifications ensure you can navigate the rigors of biopharma development, from study execution to global regulatory success in HIV and oncology.

Benefits & Perks

Gilead Sciences prioritizes employee well-being with premium benefits:

• Competitive salary estimated at $220,000–$280,000 annually, reflecting biopharma rates in Foster City with upside potential.
• Comprehensive medical, dental, vision coverage, and wellness programs.
• 401(k) with generous company match and stock options.
• Paid parental leave, flexible work arrangements, and generous PTO.
• Tuition reimbursement and leadership development opportunities.

These perks support a balanced life while advancing your career in a mission-driven company tackling HIV, oncology, and inflammatory diseases.

Career Growth

At Gilead, people leaders shape culture and employee experiences. This role positions you for advancement into senior director or VP levels, with matrix management experience building your profile. Access mentorship, training in emerging therapies, and global projects. Gilead's focus on inclusion empowers you to evolve, whether deepening clinical pharmacology expertise or expanding into strategic R&D leadership.

Pathways in HIV and Oncology

Grow by contributing to blockbuster programs in HIV antivirals and cell therapies via Kite, opening doors to influential roles in biopharma innovation.

Why Join Gilead

Joining Gilead means aligning with a company relentlessly pursuing breakthroughs in HIV, oncology, and inflammatory diseases. Foster City's vibrant campus offers cutting-edge facilities, collaborative teams, and a culture of empowerment. Make a direct impact on global health, supported by leaders who value your aspirations. With operations worldwide, you'll gain exposure to diverse therapeutic challenges and regulatory landscapes. Gilead's track record—delivering therapies that have saved millions of lives—positions you at the forefront of biopharma. If you're passionate about clinical pharmacology and ready to create possible, this is your opportunity.

Role FAQs

What is the work location?

Primarily Foster City, California, with potential for Parsippany, NJ.

What experience level is required?

Advanced degree with 5–10+ years in clinical pharmacology.

Does the role involve regulatory interactions?

Yes, representing Gilead with FDA/EMA on submissions.

What therapeutic areas?

Focus on HIV, oncology, viral hepatitis, and inflammatory diseases.

Is relocation assistance provided?

Gilead offers competitive relocation support for qualified candidates.

This role at Gilead Sciences represents a premium opportunity to lead in clinical pharmacology, driving innovations that redefine patient care.