Clinical Trials Manager
Gilead Sciences · Parsippany, NJ +1 more
Clinical OperationsFull-time$133k–$172kCompany career page
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Role summary
Gilead Sciences seeks a Clinical Trials Manager to oversee Phase II and III oncology trial execution, managing cross-functional coordination, CRO/vendor oversight, and regulatory compliance. The role requires prior oncology experience and pharmaceutical/biotech background to ensure high-quality study delivery across Parsippany, NJ or Foster City, CA locations.
What they're looking for
- 5+ years experience with BS/BA in relevant scientific discipline
- 3+ years experience with MS/MA in relevant scientific discipline
- Prior oncology clinical trials experience required
- Prior CRO, pharma, or biotech experience required
- Knowledge of FDA/EMEA regulations, ICH guidelines, and GCP standards
- Strong project management and cross-functional leadership skills
- Ability to manage multiple priorities and vendor relationships
What you'll be doing
- Coordinate and oversee all operational aspects of Phase II and III oncology clinical studies
- Manage CRO and vendor selection, contracts, budgets, and ongoing performance oversight
- Ensure protocol compliance, regulatory adherence, and timeline management across study sites
- Review and coordinate clinical study reports, case report forms, and regulatory documentation
- Train CROs, vendors, investigators, and study coordinators on study requirements and protocols
Privacy & handoff
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