Senior Statistical Programmer

Job Summary

Supporting the Biostatistics team, the fully remote Senior Statistical Programmer will develop and validate SAS programs for clinical trial reporting, implement programming standards, and collaborate with cross-functional teams to ensure compliance and quality in statistical outputs.

Key responsibilities

• Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures for clinical trials
• Implement and maintain standardized programming templates and tools for consistency and compliance across studies
• Collaborate with statisticians and clinical team members to ensure timely and high-quality deliverables

Required qualifications

• Bachelor's degree or higher in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline
• 5+ years of experience in statistical programming within the pharmaceutical, biotechnology, or medical device industry
• Proficient in SAS programming (Base, Macro, SQL) with exposure to SAS Graph and Stat procedures
• Understanding of clinical trial design, GxP principles, and FDA/EMA regulatory requirements
• Familiarity with CDISC standards (SDTM, ADaM) and ability to implement standardized datasets