Senior Statistical Programmer
Job Summary
To support clinical trial data analysis, the full-time Senior Statistical Programmer will generate tables, listings, and graphs using SAS, lead programming project teams, and ensure compliance with E-Submission Standards in a remote work environment.
Key responsibilities:
- Generate statistical tables, listings, and graphs from clinical trial databases using SAS
- Lead study or small programming project teams while utilizing the System Development Life Cycle (SDLC)
- Ensure adherence to E-Submission Standards and write specifications for SDTM and ADaM standards
Required qualifications:
- Master's degree required for all Statistics roles
- Minimum of 5 years' experience in Statistical Programming or a related field
- Expert knowledge of SAS programming, including SAS Base and SAS Macros
- Advanced understanding of ICH, 21 CFR Part 11, and ISO 9001:2000 requirements
- Hands-on experience with clinical trial and pharmaceutical development preferred
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