Clinical Trials Manager

Role: Clinical Trials Manager (CTM) supporting Gilead's Oncology pipeline, responsible for end-to-end operational delivery of Phase II and III trials. Primary objectives include ensuring high-quality study execution, managing CRO/vendor relationships, and maintaining study timelines. Responsibilities involve coordinating study activities, contributing to protocol and documentation development, overseeing site management and regulatory compliance, and supporting study budgeting. Requires strong project management, clinical, and regulatory expertise, with a focus on oncology. Qualifications: 5+ years with BS/BA or 3+ years with MS/MA in a relevant scientific discipline; prior oncology experience; experience managing CROs and clinical trials. High-value specifics include oncology (cancer), Phase II/III, CRO oversight, regulatory compliance (FDA/EMA, GCPs), and cross-functional collaboration. The role may involve travel and is based in Parsippany, NJ or Foster City, CA.