Senior Statistical Programmer - job 3 of 15

Job Summary

A company is looking for a Sr. Statistical Programmer.

Key Responsibilities

• Develop and validate SAS programs for analysis datasets, tables, listings, and figures for clinical trial reporting
• Implement and maintain standardized programming templates and tools to ensure compliance across clinical studies
• Collaborate with cross-functional teams to ensure timely and high-quality deliverables and perform quality control on datasets

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, with experience in SAS Graph and Stat procedures; knowledge of R or data visualization is a plus
• Understanding of clinical trial design and FDA/EMA regulatory requirements, particularly for medical device submissions
• Familiarity with CDISC standards (SDTM, ADaM) and ability to implement standardized datasets