The Clinical Data Programmer is responsible for designing, developing, transforming, and validating clinical study databases and data models within CDMS, DMW, and CDW
Job Summary
The Clinical Data Programmer is responsible for designing, developing, transforming, and validating clinical study databases and data models within CDMS, DMW, and CDW.
The role supports end‑to‑end clinical data management, SDTM deliverables, process improvement, automation initiatives, and cross‑functional collaboration to ensure high‑quality and compliant clinical trial data.
ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a Global Employee Assistance Programme.
Matching Summary
The Clinical Data Programmer is responsible for designing, developing, transforming, and validating clinical study databases and data models within CDMS, DMW, and CDW.
Skills & Requirements
Must-have
CDMS, DMW, CDW
SDTM staging/model transformations
SDTM dataset generation
GxP, clinical development processes
cross-functional collaboration
Nice-to-have
process improvement initiatives
automation initiatives
sharing best practices
lessons learned
enhancing efficiency
Key Requirements
M.Sc/B.Sc in Life Science, Computer Science, IT, or related field
5 years pharma experience in DMW, LSH, Veeva
Hands-on experience with CDASH, CDISC, SDTM
Experience working with global, cross-functional teams