Director, Clinical Data Management

Role: Lead clinical data management for a new radiopharmaceutical product targeting oncology indications, overseeing end-to-end data strategies and study execution. Responsibilities: develop and implement data management plans, ensure quality and timely completion of clinical trial data from study start-up to database lock, and oversee CRO/vendor performance; collaborate with cross-functional teams including Biostatistics, Clinical Operations, and Regulatory Affairs; manage data review activities, issue resolution, and documentation. Requirements: Bachelor's or Master's in Life Sciences, 10+ years of industry experience in clinical data management, expertise in EDC systems like Medidata RAVE or Veeva, solid knowledge of GCP, CDISC, and FDA regulations; experience in oncology clinical trials, managing CRO relationships, and utilizing AI tools preferred. HighValue: oncology, radiopharmaceutical modality, clinical stage (likely Phases 1-3), focus on data quality and compliance, cross-functional collaboration, remote/hybrid work with ~10% travel.