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# Senior Statistical Analyst - RWE - SAS programming

- **Company:** IRE PARTNERS, LLC
- **Location:** Nashville, TN, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, Computer Programming, Data Files, Python (Programming Language), SAS (Software), Extensible Markup Language (XML), Information Technology, Data Management
- **Published:** November 14, 2026
- **Apply:** https://www.careerbuilder.com/job-details/senior-statistical-analyst-rwe-sas-programming-nashville-tn--aeec1742-4e95-44d2-bd9e-8ddf68bd4588

## About the Role

Statistical Analysis System (SAS), Statistics, Clinical Research, International Health, Medical Products, Analysis Skills, Data Sets, Statistics, Quality Control, Biostatistics, * Degree in statistics, mathematics, computer science or related quantitative discipline, or equivalent relevant programming expertise.

 * Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
 * Proficiency in statistical software SAS (R or Python are also used in a more limited capacity)
 * Understanding of clinical trial design, statistical methodologies, and regulatory requirements.
 * Practical statistical programming experience in clinical trials using SAS or another appropriate statistical programming environment.
 * Knowledge of CDISC SDTM and ADaM standards.
 * Understanding of clinical trial data, statistical outputs and validation practices.
 * Experience developing and validating analysis datasets, tables, listings and figures.
 * Experience reviewing colleagues' work and providing technical guidance on clinical statistical programming., * Experience supporting regulatory submissions.
 * SAS programming capability (R or Python are also used in a more limited capacity)
 * Advanced CDISC or Define XML expertise.

## Description

* Develop and validate analysis datasets, tables, listings and figures.
 * Apply programming standards and specifications consistently.
 * Perform quality control and resolve data or programming issues.
 * Collaborate with biostatistics, data management and clinical stakeholders.
 * Maintain traceable programming documentation and submission readiness.
 * Provide technical guidance, peer review or mentoring on complex work within the discipline.