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# Statistical Programmer

- **Company:** Atlas Search, LLC
- **Location:** United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Coherent Remote File System (CRFS), SAS (Software), Information Technology, Data Management
- **Published:** September 30, 2026
- **Apply:** https://www.dice.com/job-detail/340a55ae-bc5c-4c9f-9c03-814e16b95b6b

## About the Role

* Bachelor's degree in Statistics, Biostatistics, Computer Science, Mathematics, Life Sciences, or a related quantitative discipline.\\n
 * Minimum of 8+ years statistical programming experience in Biotech, Pharma, or CRO industry.\\n
 * Strong knowledge of CDISC standards, including SDTM and ADaM.\\n
 * Experience overseeing vendor deliverables and supporting regulatory submissions.\\n

## Description

The Senior Statistical Programmer will independently lead programming activities for assigned clinical studies while maintaining hands-on involvement in programming, validation, and technical oversight. This role combines study-level ownership, strong knowledge of clinical study data, direct programming expertise, and oversight of internal and vendor-produced datasets, tables, listings, figures, and regulatory submission deliverables.
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Responsibilities:
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 * Lead study-level statistical programming activities, including planning, prioritization, timeline management, risk identification, and status reporting.\\n
 * Develop, program, and validate SDTM and ADaM datasets, tables, listings, and figures using SAS and, where appropriate, R.\\n
 * Collaborate closely with Biostatistics, Data Management, Clinical Operations, and other cross-functional teams to clarify requirements and resolve data, programming, and specification issues.\\n
 * Review internally and externally developed programs, datasets, outputs, and regulatory submission deliverables to ensure accuracy, traceability, consistency, and compliance with CDISC standards and regulatory expectations.\\n
 * Provide oversight and technical review of vendor deliverables, including specifications, datasets, tables, listings, figures (TFLs), define.xml, annotated CRFs, reviewer guides, transport files, and validation documentation.\\n
 * Support clinical study publications, regulatory submissions, health authority requests, and inspection-readiness activities.\\n
 * Monitor programming deliverables, dependencies, timelines, and risks, escalating significant issues and developing solutions as needed.\\n
 * Partner with cross-functional stakeholders and external vendors to ensure programming activities remain aligned with study requirements and project timelines.\\n