$133,195 – $189,640
Listed on Gilead Sciences’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role oversees the operational execution of clinical trials across assigned geographic regions or study components, managing budgets, timelines, vendor relationships, and regulatory compliance. It suits experienced life sciences professionals with project management skills and knowledge of clinical trial processes who want to drive the advancement of therapeutic development.
Our summary, not Gilead Sciences’s wording. The full posting is on their site.
Skills this role names
Log in to see which of these are already on your profile.
What they ask for
Required
- Advanced degree (MA, MS, PharmD, or PhD) with 3+ years relevant clinical or life sciences experience, or Bachelor's degree with 5+ years relevant experience, or equivalent clinical experience with team leadership
- Experience managing external vendors and contractors
- Experience leading or managing clinical studies or project teams
Nice to have
- Fast learner capable of adapting to changing priorities
- Full cycle study management experience from start-up to close-out
- Advanced knowledge of study management best practices and tools
- Understanding of FDA, EMA, and ICH guidelines and GCP requirements
- Familiarity with medical and scientific terminology
- Clear and concise communication skills
- Ability to work in team-oriented, matrixed environments
- Ability to manage multiple concurrent tasks
- Willingness to travel when needed