Clinical Program Manager

Role: Clinical Program Manager (CPM) overseeing clinical trial execution in Revolution Medicines' oncology programs, primarily related to RAS-addicted cancers. Responsibilities include leading trial management, vendor oversight, adherence to GCP, ICH, and SOP standards, and cross-functional collaboration to ensure trial timelines, budgets, and data integrity. The CPM also develops study documentation, manages CRO relationships, and mentors junior staff. Qualifications: RN, Bachelor’s, or Master’s in biological sciences or related field; 8+ years in clinical operations or research within pharma/biotech; 4+ years of study management or leadership experience. Skills: strong knowledge of FDA, ICH, GCP regulations; experience in trial startup, management, and vendor selection; proficient in project tracking tools, with some familiarity with eTMF, EDC, CTMS systems. Preferred: oncology trial experience (early/late stage), international trial operations, mentorship skills. High-Value: Oncology focus, early to late-stage trials, biologics modalities, cross-functional vendor management, and trial oversight in a fast-paced research environment. WorkSetup: onsite Redwood City, CA, with ~25% travel.