Strong knowledge of gxp and clinical development processes
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.
ICON plc fosters an inclusive environment driving innovation and excellence while offering competitive benefits including health insurance, retirement planning, and global employee assistance programs.
This role requires strong collaboration with Data Managers, Biostats, IT, and external vendors to ensure high-quality and compliant clinical trial data delivery.
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
5 years pharma experience in DMW
Hands-on experience with CDASH and CDISC
Strong knowledge of GxP and clinical development processes
Experience with Veeva and LSH systems
Proficiency in SDTM programming deliverables
Nice-to-have
Process improvement and automation initiatives
Cross-functional collaboration skills
Contribution to standards adoption
Effective stakeholder communication
Technical input on protocol requirements
Key Requirements
M.Sc/B.Sc in Life Science, Computer Science, or IT