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, and 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 include prior experience managing CROs, leading multi-phase studies in oncology or cell therapies, and 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.