onsite
Senior Statistical Programmer - Bristol Myers Squibb
Software Engineer
Lead complex statistical programming for clinical trials, leveraging SAS, R, and Python to deliver robust data analyses and reports that drive critical therapeutic decisions.
About the role
Key Responsibilities
- Design, develop, and maintain statistical programs for clinical trial data analysis using SAS, R, and Python.
- Collaborate with biostatisticians, data managers, and clinical teams to ensure accurate data extraction, cleaning, and validation.
- Generate comprehensive statistical reports, tables, figures, and listings for regulatory submissions and internal stakeholders.
- Implement and optimize SQL queries for efficient data retrieval from large clinical databases.
- Ensure compliance with GxP, FDA, and EMA guidelines, maintaining rigorous documentation and version control.
Requirements
- Advanced proficiency in SAS (Base, Macro, PROC SQL) and experience with R or Python for statistical programming.
- Strong understanding of clinical trial design, data structures, and regulatory submission requirements.
- Experience with SQL and relational database management.
- Excellent problem‑solving skills and attention to detail.
- Effective communication skills for cross‑functional collaboration.