Senior Statistical Programmer
Location: Remote
Compensation: Hourly
Reviewed: Thu, Sep 24, 2026
This job expires in: 30 days
Job Summary
Providing expert-level statistical programming support for clinical studies, the remote Senior Statistical Programmer will develop, validate, and maintain SAS programs while generating and QCing datasets and deliverables for regulatory compliance.
Key responsibilities
- Develop, validate, and maintain SAS programs, macros, and programming templates for clinical studies
- Generate and perform quality control on SDTM/ADaM datasets and Tables, Listings, and Figures (TLFs)
- Support FDA submissions and ensure compliance with CDISC standards and regulatory requirements
Required qualifications
- Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related quantitative discipline
- 10+ years of hands-on statistical programming experience in pharmaceutical, biotech, or CRO environments
- Expert-level SAS programming and SAS macro development skills
- Advanced experience with CDISC SDTM and ADaM standards
- Experience developing and validating submission-ready clinical datasets
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