{"schemaVersion":"jobsearcher.job.v1","id":"79bd2be9396c7e0a3f8a69f3","url":"https://jobsearcher.com/jobs/79bd2be9396c7e0a3f8a69f3","canonicalUrl":"https://jobsearcher.com/jobs/79bd2be9396c7e0a3f8a69f3","title":"Senior Statistical Programmer","description":"Role:Senior Statistical ProgrammerLocation: RemoteRequired Qualifications10+ years of Statistical Programming / Clinical SAS Programming experience.Strong hands-on expertise in SAS programming.Advanced experience with CDISC standards, SDTM, and ADaM.Strong experience developing and validating Tables, Listings, and Figures (TLFs).4+ years of oncology clinical trial experience required.Recent direct experience working for a pharmaceutical or biotechnology sponsor required.Strong experience supporting late-phase clinical trials and regulatory submissions.Minimum 2+ years of regulatory submission experience.Strong understanding of clinical trial data, CRFs, protocols, SAPs, and clinical study documentation.","company":"Sriven Systems","rawCompany":"sriven systems","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-09-10T09:43:10.144Z","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":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Statistical Programmer","description":"Role:Senior Statistical ProgrammerLocation: RemoteRequired Qualifications10+ years of Statistical Programming / Clinical SAS Programming experience.Strong hands-on expertise in SAS programming.Advanced experience with CDISC standards, SDTM, and ADaM.Strong experience developing and validating Tables, Listings, and Figures (TLFs).4+ years of oncology clinical trial experience required.Recent direct experience working for a pharmaceutical or biotechnology sponsor required.Strong experience supporting late-phase clinical trials and regulatory submissions.Minimum 2+ years of regulatory submission experience.Strong understanding of clinical trial data, CRFs, protocols, SAPs, and clinical study documentation.","datePosted":"2026-09-10T09:43:10.144Z","dateModified":"2026-09-10T09:43:10.144Z","hiringOrganization":{"@type":"Organization","name":"Sriven Systems","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"79bd2be9396c7e0a3f8a69f3"},"url":"https://jobsearcher.com/jobs/79bd2be9396c7e0a3f8a69f3"}}