Working under the leadership of a Programming team leader, the full-time Senior 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 client-facing role. 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; 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