Senior Statistical Programmer

Job Summary

To support clinical research projects, the full-time Senior Statistical Programmer will generate tables, listings, and graphs from clinical trial databases using SAS, while working remotely and leading programming project teams.

Key responsibilities

• Generate statistical outputs and reports from clinical trial data using SAS programming
• Lead small programming project teams and manage deliverables throughout the System Development Life Cycle (SDLC)
• Ensure compliance with E-Submission Standards and regulatory requirements, including SDTM and ADaM standards

Required qualifications

• Master's degree in Statistics or a related field
• Minimum of 5 years of experience in Statistical Programming or a similar role
• Expert knowledge of SAS programming, including SAS Base and SAS Macros
• Advanced understanding of ICH guidelines, 21 CFR Part 11, and ISO standards
• Hands-on experience with clinical trial and pharmaceutical development preferred