A company is looking for a Principal Statistical Programmer Consultant (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, ensuring compliance with regulatory requirements
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 Consultant • Fremont, California, United States