Drive end-to-end operational delivery of early-phase oncology trials.
Ensure high-quality execution through strong cross-functional leadership and CRO/vendor oversight.
Serve as a key contributor for study execution and study management by coordinating with internal teams and external partners.
Proactively identify risks and implement solutions to maintain study timelines.
Coordinate review of data listings and preparation of interim/final clinical study reports.
Ensure effectiveness of site budget/contract process.
Train CROs, vendors, investigators, and study coordinators on study requirements.
Travel is required.

Bachelor's Degree and Five Years’ Experience in a relevant scientific discipline.
OR Masters' Degree and Three Years’ Experience in a relevant scientific discipline.
Prior CRO/Pharma experience REQUIRED.
Prior Oncology experience REQUIRED.
Early Development/Early Phase Oncology experience preferred but not REQUIRED.
Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
Excellent teamwork, communication, decision-making and organizational skills are required.

Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location.
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
Company-sponsored medical, dental, vision, and life insurance plans.

Clinical Trials Manager, Early Phase Oncology

Key skills