This role provides end-to-end oversight of SDTM programming activities from study start-up through to regulatory submission
Job Summary
This role provides end-to-end oversight of SDTM programming activities from study start-up through to regulatory submission.
The successful candidate will act as a technical authority on CDISC standards ensuring quality, compliance, and consistency across trials.
ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.
Matching Summary
This role provides end-to-end oversight of SDTM programming activities from study start-up through to regulatory submission.
Skills & Requirements
Must-have
Expert SAS programming in clinical research
Advanced CDISC SDTM standards knowledge
Submission-ready package development experience
Pinnacle 21 review and compliance expertise
Define.xml and cSDRG generation skills
Nice-to-have
Mentoring junior programming resources
Experience with ADaM data structures
Strategic input on trial set-up documentation
Collaboration in matrixed FSP environments
Global cross-functional team leadership
Key Requirements
Bachelor's degree in Computer Science or related field