Principal Statistical Programmer

A company is looking for a Principal Statistical Programmer.

Key Responsibilities

Lead the development and validation of statistical programs for high-quality deliverables

Create and review programming plans and specifications, ensuring compliance with CDISC standards

Review and validate deliverables from CROs and support preparation of clinical study reports and regulatory submissions

Required Qualifications

Expert-level SAS programming skills with experience in complex programming assignments

Advanced knowledge of CDISC standards, including CDASH, SDTM, and ADaM

Experience in the drug development process and collaboration with CROs

Experience with FDA / EMEA / CDE filings

Bachelor's degree in a computational or biological science with 8 years of experience, or a Master's degree with 6 years of experience