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Statistical Programmer III/IV - Fred Hutchinson Cancer Center
Software Engineer
Senior Statistical Programmer responsible for designing, developing, and validating statistical analysis datasets and reports for clinical trials, leveraging SAS, R, and SQL to support oncology and infectious disease research.
About the role
Key Responsibilities
- Develop and maintain statistical analysis datasets and SAS programs for multi‑site clinical trials.
- Validate and troubleshoot statistical outputs, ensuring compliance with regulatory standards (FDA, EMA, ICH).
- Collaborate with biostatisticians, data managers, and clinical teams to define analysis plans and deliverables.
- Generate and review statistical reports, tables, listings, and figures (T&L) for study reports and regulatory submissions.
- Maintain documentation, version control, and audit trails for all programming activities.
Requirements
- 5+ years of experience in statistical programming within clinical research.
- Strong understanding of clinical trial design, data structures, and regulatory guidelines.
- Excellent problem‑solving skills and attention to detail.
- Effective communication and teamwork abilities in a multidisciplinary environment.