Job Description

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 models
Oversee system delivery life cycle in collaboration with appropriate...

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