Director, Clinical Pharmacology- Inflammation

About the role

Gilead Sciences is seeking a Director within the Clinical Pharmacology Group to lead clinical pharmacology studies of the highest complexity. This role offers unparalleled opportunity to be involved in every aspect of the product development process, from first-in-human trials through approval, including post-marketing activities.

Responsibilities

• Leading clinical pharmacology studies of the highest complexity
• Providing strategic leadership and demonstrating accountability for the clinical pharmacology programs supporting Phase 1-4 clinical development for development compounds in your therapeutic area
• Developing and implementing new clinical pharmacology tools and technologies to drive smarter drug development for programs
• Representing the department and providing subject matter expertise on cross-functional project teams
• Authoring/reviewing/approving clinical protocols, analysis plans, study reports and regulatory submissions
• Developing and maintaining collaborative working relationships with colleagues within and outside the department
• Evaluating departmental and broader organizational SOPs as fit for purpose, in compliance with current scientific standards and regulatory requirements
• Ensuring adherence to agreed timelines and budgets to insure prompt and accurate execution of deliverables from clinical pharmacology studies and programs
• Understanding the impact of decisions and actions on the business and consulting with colleagues and management as applicable
• Participating in and collaborating with individuals from across the business in special projects
• Developing and presenting training within and outside the department

Requirements

• At least 8 years’ experience and a PhD, PharmD or MD degree with emphasis in clinical pharmacology, pharmacokinetics or a related scientific discipline
• In-depth knowledge of pharmacokinetic and other analysis software programs (e.g. WinNonlin, GraphPad, etc.)
• Thorough knowledge of current and emerging scientific standards regulatory requirements for assigned territories
• Excellent written and oral communication skills and ability to convey complex technical information clearly
• Confidence and ability to present to and influence senior leaders
• Confidence and discipline to work autonomously
• Genuine curiosity and drive to ask questions – looking for the ‘why’ of every project
• Desire to strive for continuous improvement

Qualifications

• Experience in clinical pharmacology and related fields
• Knowledge of regulatory requirements and guidelines
• Strong analytical and problem-solving skills
• Ability to manage multiple projects simultaneously
• Excellent interpersonal and communication skills

Skills

• Expertise in pharmacokinetic and other analysis software programs
• Strong leadership and strategic planning skills
• Ability to work independently and collaboratively
• Excellent written and verbal communication skills

Benefits

The salary range for this position is: $226,185.00 - $292,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans. For additional benefits information, visit here.