Principal Statistical Programmer Consultant

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