Clinical Database Programmer
Core
Design, build, configure, test, and maintain electronic data capture (EDC) databases and clinical data management programming for clinical studies to ensure high-quality, analysis-ready data.
Role type
Clinical Database Programmer (IC)
Builds
EDC databases, edit checks, derivations, form logic, and data transfer specifications for clinical trials
Domain
Clinical Research / Pharmaceutical / Biotechnology
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SQL programming, EDC systems (Veeva CDMS/EDC), relational database design, clinical trial processes, regulatory requirements (FDA/ICH-GCP), data extraction, MedDRA/WHO Drug coding
Preferred skills
Veeva CDMS expertise, data analytics solutions, process improvement methodologies
Technologies
Veeva CDMS, Veeva EDC, SQL, SAS, Microsoft Office
Responsibilities
Lead end-to-end clinical database programming activities; Design and maintain EDC databases per study requirements; Develop edit checks and data logic; Support study milestones from start-up to database lock; Create and maintain reports and data review tools; Troubleshoot database programming issues
Seniority
Mid-level, hands-on IC
