Clinical Database Programmer
Core
Design, develop, test, and maintain clinical databases and electronic data capture (EDC) systems for pharmaceutical/biotech clinical studies.
Role type
Clinical Database Programmer (IC)
Builds
Clinical trial databases, forms, edit checks, and reports for study teams
Domain
Pharmaceutical/Biotechnology / Clinical Trials
Deliverable
production ML models | product features | dashboards & analysis
Required skills
Medidata Rave EDC expertise, C# programming, database design, requirements gathering, ICH/GCP guidelines knowledge, 21 CFR Part 11 compliance
Preferred skills
Medidata Cloud Admin, ePRO, IVRS/IWRS, CTMS, Business Objects, JReview, Cognos, Crystal Reports
Technologies
Medidata Clinical Cloud (MCC), Rave, C#, MS Project, MS Excel, Business Objects, JReview, Cognos, Crystal Reports
Responsibilities
Design/develop/test clinical databases including forms, folders, matrices, data dictionaries, edit checks, and derivations; Perform peer reviews for studies built by other programmers; Manage timely-quality deliverables for assigned protocols; Function as an EDC Subject Matter Expert providing guidance on Medidata Rave functionality
Seniority
Mid-level, hands-on IC
