Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management at Revolution Medicines, overseeing clinical trial data activities across all phases for oncology trials targeting RAS mutations. Responsibilities include managing data collection, ensuring data accuracy and completeness, vendor oversight, review of protocols and CRFs, EDC database management, and adherence to Data Management Plans. The role involves cross-functional collaboration, leadership of external vendors and internal teams, and project management of data timelines. Requirements: MS/BS degree, 11+ years' experience in designing and executing clinical trials, strong knowledge of clinical databases, medical coding, GCP, FDA, ICH regulations, with industry experience essential. Preferred: oncology experience, especially in solid tumors, and 5+ years of line management. High-value: oncology, RAS inhibitors in clinical development, focus on trial data integrity and vendor coordination. Work setup: onsite in Redwood City, CA, salary range $186K–$233K, with focus on leadership, compliance, and technical expertise.