Associate Director, Clinical Data Management
Core
Leadership role overseeing clinical data management for the R&D pipeline, ensuring high-quality data delivery for late-phase studies and complex clinical development projects.
Role type
Senior IC clinical data management program lead with line management responsibilities
Builds
Clinical trial data deliverables for drug development programs
Domain
Pharmaceutical / Clinical Research
Required skills
Clinical drug development process knowledge, EDC systems expertise, project management, data quality oversight, vendor management, regulatory guidelines knowledge, resource forecasting, team coaching
Preferred skills
PMP certification, late-phase study management experience, advanced degree, knowledge of eCOA and Safety Gateway systems
Technologies
Medidata RAVE, Microsoft Office, EDC systems, eCOA, Safety Gateway
Responsibilities
Provide program oversight for a group of studies and Data Management Leads; Establish governance frameworks for risk monitoring; Manage resource assignments and forecast future resource needs; Lead or support Health Authority inspections and audits; Author and review DM-related study plans and procedural documents; Provide leadership to align on data collection requirements for complex projects; Mentor staff and develop next-generation leaders.