Associate Director, Clinical Operations Compliance & Training

Role: Associate Director responsible for Clinical Compliance and GCP systems oversight within Revolution Medicines' late-stage oncology clinical programs, focusing on RAS-targeted therapies. Responsibilities: develop and implement GCP systems, clinical policies, SOPs, and training; ensure inspection readiness; support audit and inspection activities; collaborate with QA and cross-functional teams on quality initiatives and continuous improvement; oversee clinical study compliance; and manage line reports. Qualifications: Bachelor's in biological sciences or health-related field; 10+ years in clinical compliance, quality assurance, or clinical operations in pharma/biotech; strong knowledge of FDA, ICH, GCP, and ex-US regulations; proven experience in SOP development, oversight activities, and audit responses; exceptional analytical, organizational, and communication skills. Preferred: oncology experience (early/late-stage), line management skills, RN or master's degree, familiarity with ex-US agencies. HighValue: focus on GCP compliance, inspection readiness, and clinical quality in late-stage oncology trials, supporting RAS-targeted therapies. WorkSetup: onsite in Redwood City, CA, with ~25% travel.