Veeva Edc Developer

Location : Remote

Experience : 6+ Years

Educational Qualifications

Bachelor's degree or related experience

Job Purpose :

This position requires the following critical abilities :

• Knowledge of the drug development process.
• 6+ years’ experience in Data Management, Clinical Programming, or other Clinical Research related fields, with a minimum of 4 years’ experience in EDC programming
• Hands-on experience with Veeva(mandatory), Medidata Rave, Oracle Inform, etc.
• Experience programming in CQL, CDB, working with JSON format and / or C# is preferred
• Experience integrating other clinical trial modules (eg : lab, safety, IRT, coding, etc.) with the EDC system
• Understanding of industry standard technologies to support Clinical Development needs (e.G. CTMS, SAS, R or Python, Data Warehouses, SharePoint)
• Manage edit check specifications and configure edit checks at the trial level
• Execute UAT scripts to test the setup of the clinical study or EDC Platforms
• Configure different instances of study (eg : UAT, production, testing etc.,)
• Facilitate user access requests for study teams
• Set up and manage blinded and unblinded study configurations in EDC
• Serve as SME for all EDC database-related activities at the trial level
• Set up, configure, validate, and integrate other modules within the EDC ecosystem