> Markdown version of [/jobs/ext/3971196-statistical-programmer](https://www.wearedevelopers.com/jobs/ext/3971196-statistical-programmer). 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). --- # Statistical Programmer - **Company:** Katalyst Talent Agency - **Location:** Atlanta, GA, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Bioinformatics, Coherent Remote File System (CRFS), R (Programming Language), SAS (Software), Extensible Markup Language (XML) - **Published:** October 27, 2026 - **Apply:** https://www.careerjet.com/job/uscf284afb3a9a0f3bba31b2eae1bb0b78/eaa ## About the Role * B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields * Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group * At least 6 years of Clinical trials related work experience in SAS programming, analysis and reporting in the context of drug development projects is required * Well experienced in Pinnacle21 validation process, generating define xml using Pinnacle 21 * Extensive experience in implementing CDISC standards, as well as annotating CRFs, creating specifications for SDTM and ADaM datasets * Experienced in creating Define.xml and the corresponding Reviewers' Guide for SDTM and ADaM datasets * Good verbal and written communications skills in English * Demonstrated knowledge of clinical drug development * Proficiency in conducting advanced statistical analyses * Must be independent, attention to detail, accountable to quality and timely delivery * Ability to work on multiple collaborative projects, team player mentality ## Description * As a Statistical Programming Consultant, you will use your SAS and R programming skills to prepare SDTM and ADaM datasets, Tables, Listings, & Figures (TLFs), as well as create related documents such as aCRF, programming specifications, and define packages (including reviewer's guides) for Phase 1 to Phase 4 clinical trials * In addition, you will conduct quality control and quality assurance activities on datasets and outputs and may participate in company initiatives to improve the efficiency of end-to-end statistical programming activities, analysis, and reporting (IT, methodology, automation, quality) * You will work closely in teams led by statistical programmers, statisticians, and drug development consultants, supporting a variety of client projects across various therapeutic areas and complexities