Director, Clinical Data Management

Role: Director of Clinical Data Management at a biopharma oncology company focusing on RAS inhibitors, responsible for overseeing clinical trial data activities across all phases. Core responsibilities include managing CDM tasks, vendor oversight, and ensuring data quality, accuracy, and compliance with GxP, FDA, and ICH guidelines. The role involves collaboration with CROs, data vendors, and cross-functional teams, including review and development of CRFs, management of EDC systems, and adherence to Data Management Plans. Requirements: MS, BS/BA or relevant qualification; 15+ years of experience in designing and executing clinical trials, with strong knowledge of clinical data standards, medical coding, and regulatory guidelines. Preferred: Oncology experience, especially in solid tumors, and 5+ years of line management. High-value specifics include expertise in early and late-stage trials, clinical database management, and a leadership role in a high-energy, innovative environment. The position is based at headquarters in Redwood City, CA, with a salary range of $211,000–$264,000, and involves stakeholder management, regulatory compliance, and process development.