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
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