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 mode...
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