$165,495 – $235,620
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 manages the end-to-end execution of clinical trials across multiple therapeutic areas at a pharmaceutical company, overseeing budgets, timelines, vendor relationships, and cross-functional teams while ensuring regulatory compliance. It suits experienced professionals in clinical operations who want to drive large-scale research programs and develop leadership capabilities.
Our summary, not Gilead Sciences’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in life sciences or nursing with 8+ years clinical/related experience, OR Master's/PharmD/PhD with 6+ years clinical/related experience
- Minimum 4 years cross-functional study management or leadership experience managing study or project teams
- Experience developing RFPs and selecting/managing CROs or vendors
- Ability to start-up, manage and close-out clinical studies and author regulatory documentation
Nice to have
- Advanced knowledge of specific disease or therapeutic areas
- Complete knowledge of full study lifecycle from start-up to close-out
- Advanced knowledge of study management best practices and tools
- Thorough knowledge of FDA, EMA, ICH guidelines and GCP
- Proven clinical documentation authoring ability
- Ability to lead and influence programs and initiatives
- Strong interpersonal and team dynamics understanding
- Experience in matrixed environments
- Coaching and performance management effectiveness
- Change management experience
- Travel ability as required