Senior Clinical Program Manager

Role: Senior Clinical Program Manager overseeing clinical trial execution within Revolution Medicines' oncology programs, focusing on RAS-addicted cancers. Responsibilities include leading study teams, ensuring compliance with GCP, ICH, and SOP guidelines, managing timelines and budgets, selecting and managing CROs/vendors, analyzing data metrics, and driving risk mitigation. The role involves developing study documentation, influencing cross-functional stakeholders, and possibly leading interdepartmental strategic initiatives. Qualifications: RN or bachelor's/master's in biological sciences or health-related field; 10+ years in clinical operations or research, with at least 6 years in study management or team leadership. Expertise in FDA regulations, GCP, ICH guidelines, and clinical trial startup, management, and closure required. Preferred: experience with oncology, early/late-stage trials, vendor systems (eTMF, EDC, CTMS), and managing direct reports. High-value specifics include oncology indication, clinical trial phases, global/regional operations, and a hybrid onsite location in Redwood City, CA, with ~25% travel.