Clinical Program Manager

Role: Lead and oversee global Clinical Operations for Gilead/Kite's oncology programs, focusing on the execution of Phase I-IV clinical trials across multiple therapeutic areas. Responsibilities include managing study teams, resource allocation, vendor management (including CROs), study start-up through close-out, and ensuring compliance with SOPs, GxP, and regulatory standards (FDA, EMA, ICH). The role involves strategic planning, budget oversight, risk mitigation, and cross-functional collaboration to support the development and commercialization of innovative cancer immunotherapies, particularly CAR T-cell therapies. Qualifications: Bachelor's degree with 8+ years (or advanced degrees with fewer years) in clinical research or life sciences, including experience in study management, vendor selection, and team leadership. Preferred skills encompass deep knowledge of regulatory guidelines, experience in hematological malignancies or oncology, and proficiency with clinical trial management tools. The position requires strong leadership, communication, organizational skills, and the ability to mentor teams within a highly matrixed environment. It involves direct line management of study management professionals and may include strategic input on operational planning. Work setup may involve travel, with an emphasis on fostering inclusion, talent development, and empowering teams in a global, innovative biopharma setting.