Senior Statistical Programmer
Job Summary
Working remotely from any location in Mexico, the full-time Senior Statistical Programmer will generate tables, listings, and graphs from clinical trial databases using SAS while leading study or small programming project teams.
Key responsibilities
- Generate and manage statistical outputs from clinical trial databases utilizing SAS programming
- Lead programming deliverables following the System Development Life Cycle (SDLC) and ensure compliance with E-Submission Standards
- Write specifications for SDTM and ADaM standards, and support data set pooling for submissions
Required qualifications
- Master's degree in Statistics or a related field
- Minimum of 5 years' experience in Statistical Programming or a similar role
- 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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