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# Statistical Programmer

- **Company:** ACL Digital
- **Location:** United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** SAS (Software), User-Centered Design, Data Management
- **Published:** October 8, 2026
- **Apply:** https://www.thejobnetwork.com/job/7957c4b8-7281-4a7f-84a2-d05651420139/senior-statistical-programmer-oncology

## About the Role

ACL Digital is seeking an experienced, highly autonomous Senior Statistical Programmer with 9 to 12 years of clinical trial programming expertise to join our life sciences practice on a long-term contract basis.

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In this role, you will work closely with biostatistics, data management, and clinical teams to lead and execute statistical programming deliverables across Phase I-IV clinical trials, with a primary focus on Oncology. The ideal candidate must have direct experience working inside a Sponsor / Pharmaceutical organization environment and demonstrate an advanced command of CDISC standards, complex SAS programming, and global regulatory submission packages., 9 to 12 years of progressive SAS statistical programming experience in Pharma, Biotech, or CRO environments., Mandatory: Direct experience working within a Sponsor / BioPharma company environment (handling in-house submission pipelines and internal stakeholder communication)., Expert knowledge of CDISC standards (SDTM, ADaM implementation, Define.xml, Pinnacle 21 validation tools)., Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related quantitative field.

## Description

Advanced SAS (Base SAS, SAS/STAT, SAS/GRAPH, SAS/MACRO). Hands-on experience with R for statistical reporting or open-source submission workflows is a strong plus.