Act as the customer and clinical site trusted advisor to ensure that the study trial design is configured to meet the customer’s goals and offer full benefits of Veeva’s CDMS application while providing training and mentorship Work and consult with customers to review and understand clinical protocol requirements and all project specifications, applying industry and Veeva best practices Drive database development activities per implementation project plan by working with various members of the sponsor, CRO, and other external vendor teams Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and configure transfers based on requirements Configure forms, rules, and other study items with Veeva Vault CDMS product during development and develop custom listings based on customer data cleaning requirements using SQL-based language Conduct on-site or remote user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study Support requirements gathering and specification creation process for all study integrations and go-live activities to ensure a smooth transition of the study to the customer Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Veeva procedural requirements Participate and contribute to process product or best practices initiatives and support developers and testers during the project lifecycle Participate in Vault CDMS Product team discussions to convey data management activities, challenges, and end-user expectations Configure and support data ingestions (imports) into Veeva CDB