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# Senior Statistical Programmer

- **Company:** Simulstat Inc.
- **Location:** United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Data Validation, SAS (Software), SQL Databases, Extensible Markup Language (XML), Information Technology, Data Management
- **Published:** May 14, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=9780a4c6931642b4

## About the Role

Do you have experience in XML?, Do you have a Bachelor's degree?, * Bachelor's degree or higher in a quantitative discipline (Statistics, Mathematics, Computer Science, or similar)

 * Four or more years of SAS programming in a pharma or CRO setting across Phase I-IV trials; Phase 3 pivotal trial experience required, rare disease or orphan drug exposure a plus
 * Proficiency in SDTM, ADaM, and Define.XML; working knowledge of CDISC/CDASH, eCTD, and applicable regulatory guidelines (FDA, ICH, GCP)
 * Strong SAS skills across ODS, SQL, Macro, Stat, and Graph; expertise with R a plus
 * Comfortable managing competing priorities across multiple active studies in a fast-moving environment

## Description

* Program and validate SDTM/ADaM datasets supporting a Phase 3 pivotal trial, including longitudinal lab endpoints and averaged-timepoint primary endpoint derivations
 * Develop, execute, and QC TFLs; review and validate outputs generated by CRO and vendor partners
 * Perform dataset compliance reviews against CDISC standards across active study phases; maintain Define.XML
 * Develop data validation programs to support the Data Management team throughout study conduct
 * Periodically re-run and verify existing code to ensure ongoing program integrity across multiple related studies


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