• Directly contributes to the oversight of Data Management service providers and external vendors on assigned studies and programs, ensuring milestones and quality deliverables are achieved on time, within budget, and in accordance with regulatory requirements. • Serves as the point of contact for decision making and resolution within and across studies and programs. • Reviews and approves Data Management related documentation for quality, completeness, and accuracy; • Performs secondary User Acceptance Testing (UAT) of the EDC system prior to deployment to the production environment. • Contributes to and oversee the development of the Integrated Oversight Plan, establishing an internal cross-functional oversight plan to ensure data quality and demonstrate oversight; conducts DM data review per the plan using appropriate tools and systems. • Ensures the timely provisioning of feedback on draft protocols, risk assessments, and functional area plans and outputs as appropriate. • Participate in continual development through the acquisition and enhancement of knowledge related to drug development, clinical trials methodology, and DM best practices, and apply the information to make recommendations for improvement to processes and business performance.