remote
Principal Statistical Programmer US, CAD, UK only - Syneos Health
Software Engineer
Lead complex statistical programming for global clinical trials, driving data integrity and regulatory compliance using SAS, R, and SQL across multiple therapeutic areas.
About the role
Key Responsibilities
- Design, develop, and validate statistical programs for clinical trial data management and analysis.
- Collaborate with biostatisticians, data managers, and clinical teams to ensure accurate and timely data outputs.
- Lead code reviews, troubleshoot issues, and implement best practices for reproducibility and documentation.
- Prepare and review statistical tables, listings, and figures for regulatory submissions (IND, NDA, BLA).
- Mentor junior programmers and contribute to continuous improvement of programming standards.
Requirements
- 10+ years of experience in statistical programming within the life sciences industry.
- Expertise in SAS (Base, Macro, PROC SQL) and proficiency in R for advanced analytics.
- Strong understanding of clinical trial design, data structures, and regulatory guidelines (FDA, EMA).
- Excellent problem‑solving skills, attention to detail, and ability to work independently in a fast‑paced environment.
- Effective communication skills and experience mentoring junior staff.