Key Accountabilities:

• Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process
• Create edit check specifications and program or modify checks at study level within EDC
• 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 database related activities
• Setup, configure, unit test and functionally validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc.,
• Familiar with custom functions within EDC systems
• Work closely with EDC vendors regarding any tool related issues in the system
• Ability to troubleshoot database setup as per study needs
• Prepare, test and implement post production changes as per study needs
• Arc...