Senior Statistical Programmer Consultant

Job Summary

Working closely with a single sponsor, the full-time Senior Statistical Programmer Consultant will develop, validate, and maintain SAS programs for clinical study data analysis and reporting in a remote environment.

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
• Collaborate with Biostatistics, Data Management, and Clinical teams to ensure quality deliverables meet project timelines

Required qualifications:

• Bachelor's degree in computer science, statistics, or related scientific disciplines with 5 years of clinical programming experience, or a Master's degree with 6 years of experience
• Strong SAS programming experience within the pharmaceutical/CRO industry
• Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
• Good understanding of CDISC standards and clinical trial processes
• Experience supporting regulatory submissions is preferred