> Markdown version of [/jobs/ext/4703026-senior-statistical-analyst-rwe-sas-programming](https://www.wearedevelopers.com/jobs/ext/4703026-senior-statistical-analyst-rwe-sas-programming). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Statistical Analyst - RWE - SAS programming - **Company:** 410 ICR United States USA - **Location:** Wilmington, NC, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Clinical Data Management, Computer Programming, Python (Programming Language), SAS (Software), Extensible Markup Language (XML), Information Technology, Data Management - **Published:** November 13, 2026 - **Apply:** https://www.thejobnetwork.com/job/bc3509f5-686d-4626-85f7-65f739dd93f4/senior-statistical-analyst-rwe-sas-programming ## About the Role * 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.