{"schemaVersion":"jobsearcher.job.v1","id":"fa566ced4ea8bcf32f7bffc9","url":"https://jobsearcher.com/jobs/fa566ced4ea8bcf32f7bffc9","canonicalUrl":"https://jobsearcher.com/jobs/fa566ced4ea8bcf32f7bffc9","title":"Sr Statistical Programmer","description":"We are seeking a highly skilled Senior Statistical Programmer. This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures (TLFs) in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases I–III) and working closely with Biostatisticians, Data Management, and Clinical teams to deliver high-quality outputs for regulatory submissions.QualificationsEducation: Master’s degree in Statistics requiredRequired SkillsProficiency in SAS programming (Base, Macro, SQL).Strong knowledge of CDISC SDTM and ADaM implementation guidelines.5+ years of statistical programming experience in the pharmaceutical/biotech/CRO industry.Experience with regulatory submissions (FDA, EMA, PMDA) preferred.Lead and Client facing experience preferredPreferred SkillsExcellent problem-solving skills, attention to detail, and ability to manage multiple priorities.Strong communication skills and ability to work in a collaborative, fast-paced environment.","company":"Connect Life Sciences","rawCompany":"connect life sciences","city":"Cary","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-04-25T12:32:45.698Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr Statistical Programmer","description":"We are seeking a highly skilled Senior Statistical Programmer. This is a lead role and will be responsible for the end-to-end programming and validation of clinical trial datasets, tables, listings, and figures (TLFs) in compliance with regulatory standards. The ideal candidate will have extensive experience supporting oncology clinical trials (Phases I–III) and working closely with Biostatisticians, Data Management, and Clinical teams to deliver high-quality outputs for regulatory submissions.QualificationsEducation: Master’s degree in Statistics requiredRequired SkillsProficiency in SAS programming (Base, Macro, SQL).Strong knowledge of CDISC SDTM and ADaM implementation guidelines.5+ years of statistical programming experience in the pharmaceutical/biotech/CRO industry.Experience with regulatory submissions (FDA, EMA, PMDA) preferred.Lead and Client facing experience preferredPreferred SkillsExcellent problem-solving skills, attention to detail, and ability to manage multiple priorities.Strong communication skills and ability to work in a collaborative, fast-paced environment.","datePosted":"2026-04-25T12:32:45.698Z","dateModified":"2026-04-25T12:32:45.698Z","hiringOrganization":{"@type":"Organization","name":"Connect Life Sciences","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Cary","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fa566ced4ea8bcf32f7bffc9"},"url":"https://jobsearcher.com/jobs/fa566ced4ea8bcf32f7bffc9"}}