Senior Statistical Programmer - job 2 of 4

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 trials
• Implement and maintain programming standards and templates to ensure consistency and compliance across studies
• Collaborate with cross-functional teams to ensure timely and high-quality deliverables, including quality control of 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 (Base, Macro, SQL); experience with R or data visualization is a plus
• Understanding of clinical trial design and FDA/EMA regulatory requirements for medical device submissions
• Familiarity with CDISC standards (SDTM, ADaM) and ability to implement standardized datasets