A company is looking for a Principal Statistical Programmer Consultant in Oncology.
Key Responsibilities
Lead programming activities for oncology clinical trials across multiple studies
Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines
Prepare submission-ready programming outputs and documentation for regulatory submissions
Required Qualifications
Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field
8-12+ years of statistical programming experience in pharma / biotech or CRO
Expert-level proficiency in SAS
Strong understanding of CDISC SDTM and ADaM standards
Significant experience supporting oncology clinical trials and regulatory submissions
Principal Statistical Programmer Consultant • San Francisco, California, United States