Principal Statistical Programmer Consultant

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