California Licensed Senior Statistical Programmer

Job Summary

Working remotely on a contract basis, the California Licensed Senior Statistical Programmer will develop and validate SAS programs, support late-phase oncology clinical trial submissions, and collaborate with cross-functional teams while ensuring regulatory compliance.

Key responsibilities

• Develop and validate SAS programs and datasets, including SDTM and ADaM standards
• Support late-phase oncology clinical trial submissions and regulatory deliverables
• Create, maintain, and review statistical outputs including listings, tables, figures, and analysis datasets

Required qualifications

• 10+ years of statistical programming experience in clinical research or pharmaceutical/biotech environments
• Strong oncology experience, including solid tumor studies and understanding of RECIST criteria
• Experience with late-phase clinical trials and regulatory submissions
• Proficiency in SAS programming, including SDTM and ADaM dataset development
• Experience producing TLFs (tables, listings, and figures) for clinical and regulatory reporting