Senior Director, Clinical Data Management

Role: Senior Director, Head of Data Management, leading clinical data management activities within oncology development. Responsibilities: oversee data strategies across studies, ensure high-quality, compliant data deliverables, and drive process standardization; manage vendor relationships and team development; support NDA submissions with database lock and inspection readiness; collaborate cross-functionally with Clinical Operations, Biostatistics, and Safety to align data strategies. Qualifications: minimum 12 years in data management within pharma/biotech/CRO, with extensive experience in oncology; bachelor's or master's in Life Sciences, Computer Science, or related fields; expertise in EDC systems (Medidata RAVE, Veeva), GCP, CDISC/CDASH, FDA regulations; proven leadership and vendor management skills. Preferred: Radiopharmaceutical experience, Veeva EDC familiarity, AI tools utilization. High-Value: oncology focus, radiopharmaceutical modality, clinical phase stages supporting NDA/regulatory activities. Work Setup: remote in the U.S., with no travel specified.