Clinical Program Manager

Role Lead and oversee clinical operations for Gilead's cancer therapies, ensuring the successful execution of Phase I-IV trials across multiple therapeutic areas. Responsibilities manage clinical study teams oversee study timelines, budgets, and vendor relationships contribute to study and regulatory documentation lead cross-functional study management teams engage in process improvements and organizational initiatives Requirements Bachelor's degree with 8+ years or Master's with 6+ years of clinical study management experience PhD/PharmD preferred comprehensive knowledge of GxP, FDA/EMA regulations, ICH guidelines, and clinical trial processes Preferred qualifications prior experience managing CROs leading multi-phase studies in oncology or cell therapies strong leadership skills High-value specifics focus on innovative cancer immunotherapies, including CAR T-cell therapies, with responsibilities spanning study start-up to close-out. Experience in biologics, cell/gene therapy, or related modalities is advantageous. Collaboration leading cross-functional teams, including study management and vendors, with global trial oversight. Work setup not explicitly specified; travel may be required. #J-18808-Ljbffr