Principal Statistical Programmer Consultant

Job Summary

Working directly with a single sponsor, the full-time Principal Statistical Programmer Consultant will develop, validate, and maintain SAS programs for clinical study data analysis and reporting, while collaborating with cross-functional teams in a remote setting.

Key responsibilities:

• Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
• Create datasets, tables, listings, and figures according to study requirements
• Ensure programming deliverables meet quality standards and project timelines

Required qualifications:

• Bachelor's degree in computer science, statistics, or related scientific disciplines with 5 years of clinical programming experience; Master's degree with 8 years of experience preferred
• Strong SAS programming experience within the pharmaceutical/CRO industry
• Hands-on experience supporting Cardiovascular, Renal & Metabolism (CVRM) studies
• Good understanding of CDISC standards and clinical trial processes
• Experience supporting regulatory submissions is preferred