Job Title

Location: Remote Experience: 4+ 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