Director, Clinical Pharmacology- Inflammation
Gilead Sciences
August 15, 2026
On-site
San Francisco Bay Area
Clinical Research and Development
Director, Clinical Pharmacology (Inflammation)
Site-based role at global headquarters in Foster City, CA.
Your Tasks And Responsibilities Will Include
- Lead clinical pharmacology studies of the highest complexity.
- Provide strategic leadership and accountability for clinical pharmacology programs supporting Phase 1–4 clinical development.
- Develop and implement new clinical pharmacology tools and technologies to drive smarter drug development.
- Provide subject matter expertise on cross-functional project teams.
- Maintain collaborative working relationships within and outside the department.
- Author/review/approve clinical protocols, analysis plans, study reports, and regulatory submissions.
- Develop high-quality clinical pharmacology plans and content for global regulatory submissions, including INDs, IBs, NDAs, MAAs, and pediatric plans.
- Evaluate SOPs for fit for purpose in compliance with scientific standards and regulatory requirements.
- Ensure adherence to agreed timelines and budgets for clinical pharmacology deliverables.
- Assess business impact of decisions and consult with colleagues/management as applicable.
- Participate in special projects across the business.
- Develop and present training within and outside the department.
Specific Education, Experience And Skills Required For This Role
- At least 8 years’ experience and a PhD, PharmD, or MD degree with emphasis in clinical pharmacology, pharmacokinetics, or related scientific discipline.
- In-depth knowledge of pharmacokinetic and analysis software (e.g., WinNonlin, GraphPad).
- Thorough knowledge of current and emerging scientific standards and regulatory requirements for assigned territories.
- Excellent written and oral communication skills; ability to convey complex technical information.
- Ability to present to and influence senior leaders.
- Ability to critically analyze problems and provide creative solutions.
- Confidence and discipline to work autonomously.
- Curiosity and drive to ask questions.
- Desire for continuous improvement.
Compensation/Benefits
- Salary range: $226,185.00–$292,710.00.
- May be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and company-sponsored medical, dental, vision, and life insurance plans.
Application Instructions
- For current employees/contractors: apply via the Internal Career Opportunities portal in Workday.
Site-based role at global headquarters in Foster City, CA.
Your Tasks And Responsibilities Will Include
- Lead clinical pharmacology studies of the highest complexity.
- Provide strategic leadership and accountability for clinical pharmacology programs supporting Phase 1–4 clinical development.
- Develop and implement new clinical pharmacology tools and technologies to drive smarter drug development.
- Provide subject matter expertise on cross-functional project teams.
- Maintain collaborative working relationships within and outside the department.
- Author/review/approve clinical protocols, analysis plans, study reports, and regulatory submissions.
- Develop high-quality clinical pharmacology plans and content for global regulatory submissions, including INDs, IBs, NDAs, MAAs, and pediatric plans.
- Evaluate SOPs for fit for purpose in compliance with scientific standards and regulatory requirements.
- Ensure adherence to agreed timelines and budgets for clinical pharmacology deliverables.
- Assess business impact of decisions and consult with colleagues/management as applicable.
- Participate in special projects across the business.
- Develop and present training within and outside the department.
Specific Education, Experience And Skills Required For This Role
- At least 8 years’ experience and a PhD, PharmD, or MD degree with emphasis in clinical pharmacology, pharmacokinetics, or related scientific discipline.
- In-depth knowledge of pharmacokinetic and analysis software (e.g., WinNonlin, GraphPad).
- Thorough knowledge of current and emerging scientific standards and regulatory requirements for assigned territories.
- Excellent written and oral communication skills; ability to convey complex technical information.
- Ability to present to and influence senior leaders.
- Ability to critically analyze problems and provide creative solutions.
- Confidence and discipline to work autonomously.
- Curiosity and drive to ask questions.
- Desire for continuous improvement.
Compensation/Benefits
- Salary range: $226,185.00–$292,710.00.
- May be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and company-sponsored medical, dental, vision, and life insurance plans.
Application Instructions
- For current employees/contractors: apply via the Internal Career Opportunities portal in Workday.