Senior Statistical Programmer Consultant
Job Summary
To support a client-focused programming effort, 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 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
- 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 Master's degree with 6 years of experience
- Strong SAS programming experience within the pharmaceutical/CRO industry
- Hands-on experience supporting Cardiovascular, Renal, and Metabolism studies
- Good understanding of CDISC standards and clinical trial processes
- Experience supporting regulatory submissions is preferred
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