Senior Consultant - Clinical Data Programming

Responsibilities

• Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship along the way
• Work with customers to interpret clinical protocol requirements and project specifications, applying industry and Veeva best practices
• Lead database development activities per the project plan, coordinating with sponsor, CRO, and other vendor teams
• Coordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data transfers
• Configure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings for customer data cleaning needs
• Run on-site or remote user acceptance testing, managing feedback, issue resolution, and study acceptance
• Support requirements gathering and specification writing for study integrations and go-live activities
• Flag risks and contingency plans to project management to keep the project compliant with regulatory and Veeva procedures
• Contribute to process, product, and best-practice initiatives, and support developers and testers throughout the project lifecycle
• Share data management activities, challenges, and end-user feedback with the Vault CDMS product team

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