Job Description
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...