Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management, leading or supporting clinical trial data activities within Genmab's development projects. Responsibilities: oversee trial data collection, validation, vendor management, and compliance, providing expertise in data management processes, standards (e.g., CDISC SDTM), and regulatory requirements; lead cross-functional data management initiatives, mentor colleagues, and represent data management in operational fora; support development and optimization of data management strategies and systems. Requirements: Bachelor's in science or related field; 10+ years in clinical data management in biotech/pharma, with extensive experience across all trial phases, including early and late-stage submissions; advanced knowledge of DM processes, systems, and CDISC standards; demonstrated leadership in cross-functional teams; solid understanding of GCP, SOPs, and global regulatory standards. High-value: senior-level expertise in clinical data management, experience with complex interdependent activities (protocol development, data review, analysis), and vendor oversight. Work setup: not specified, but extensive stakeholder engagement and cross-team coordination implied.