Job Title

Location: RemoteExperience: 6+ YearsEducational QualificationsBachelor's degree or related experienceJob 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