Expert Veeva EDC Programmer

• Create eCRF specifications, design, develop and validate clinical trial setup process
• Create edit check specifications and setup edit checks at trial level
• Implement UAT scripts to test the setup of the clinical study
• Setup different instances of study URL(eg: UAT, production, testing etc.,)
• Setup and configure user accounts for study teams
• Setup and manage blinded and unblinded study configurations
• Be the SME for all EDC database related activities
• Setup, configure, validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc.,
• Understanding of when custom functions are required within EDC systems
• Ability to troubleshoot database setup as per study needs
• Prepare, test and implement post production changes as per study needs
• Partner with appropriate team members to establish technology standards and governance mode...

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