{"schemaVersion":"jobsearcher.job.v1","id":"1d2c258cadeaccf349a4cd09","url":"https://jobsearcher.com/jobs/1d2c258cadeaccf349a4cd09","canonicalUrl":"https://jobsearcher.com/jobs/1d2c258cadeaccf349a4cd09","title":"Analyst, Statistical Programming","description":"Analyst, Statistical Programming (JN -092026-431039) Irvine, California\nSalary: USD45 - USD55.6 per hour\n\nW-2 Contract Role\n\nDuration - 6 Months\n\nLocation - Irvine, CA 92614\n\nPay Range - $45 to $55.60/hour doe\n\nSummary\nThe main function of an analyst is to support clinical research activities by developing, validating, and maintaining clinical study datasets, tables, figures, and listings. This role works closely with Biostatistics, Clinical Data Management, and cross-functional study teams to support regulatory submissions, scientific publications, routine reporting, and clinical study analyses.\n\nJob Responsibilities\n\nDevelop and validate SDTM and ADaM datasets from clinical study data.\n\nCreate, maintain, and validate SAS and/or R programs for data processing and statistical reporting.\n\nGenerate and quality check Tables, Figures, and Listings (TFLs) for clinical study reports, regulatory submissions, publications, and presentations.\n\nSupport data review, analysis data readiness, routine reports, safety reporting, and ad hoc analyses.\n\nParticipate in the implementation of Statistical Analysis Plans (SAPs) and programming specifications.\n\nEnsure compliance with company standards, quality procedures, and regulatory requirements.\n\nCollaborate with Biostatistics, Clinical Data Management, Clinical Development, Clinical Safety, and Medical Affairs teams to support study deliverables.\n\nContribute to programming standards, automation, utility macros, and process improvement initiatives.\n\nQualifications\n\nBachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, Life Sciences, or a related field.\n\n2-4 years of experience with SAS programming; knowledge of R is preferred.\n\nUnderstanding of clinical trial data, statistical reporting, and regulatory requirements.\n\nKnowledge of CDISC SDTM and ADaM standards preferred.\n\nStrong analytical, problem-solving, and communication skills.\n\nAbility to manage multiple priorities and work effectively in a collaborative team environment.\n\n#J-18808-Ljbffr","company":"Ultimate Staffing","rawCompany":"ultimate staffing","city":"Irvine","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-09-23T04:29:42.575Z","occupations":[{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"43-9111.00","title":"Statistical Assistants","slug":"statistical-assistants"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"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":"Analyst, Statistical Programming","description":"Analyst, Statistical Programming (JN -092026-431039) Irvine, California\nSalary: USD45 - USD55.6 per hour\n\nW-2 Contract Role\n\nDuration - 6 Months\n\nLocation - Irvine, CA 92614\n\nPay Range - $45 to $55.60/hour doe\n\nSummary\nThe main function of an analyst is to support clinical research activities by developing, validating, and maintaining clinical study datasets, tables, figures, and listings. This role works closely with Biostatistics, Clinical Data Management, and cross-functional study teams to support regulatory submissions, scientific publications, routine reporting, and clinical study analyses.\n\nJob Responsibilities\n\nDevelop and validate SDTM and ADaM datasets from clinical study data.\n\nCreate, maintain, and validate SAS and/or R programs for data processing and statistical reporting.\n\nGenerate and quality check Tables, Figures, and Listings (TFLs) for clinical study reports, regulatory submissions, publications, and presentations.\n\nSupport data review, analysis data readiness, routine reports, safety reporting, and ad hoc analyses.\n\nParticipate in the implementation of Statistical Analysis Plans (SAPs) and programming specifications.\n\nEnsure compliance with company standards, quality procedures, and regulatory requirements.\n\nCollaborate with Biostatistics, Clinical Data Management, Clinical Development, Clinical Safety, and Medical Affairs teams to support study deliverables.\n\nContribute to programming standards, automation, utility macros, and process improvement initiatives.\n\nQualifications\n\nBachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, Life Sciences, or a related field.\n\n2-4 years of experience with SAS programming; knowledge of R is preferred.\n\nUnderstanding of clinical trial data, statistical reporting, and regulatory requirements.\n\nKnowledge of CDISC SDTM and ADaM standards preferred.\n\nStrong analytical, problem-solving, and communication skills.\n\nAbility to manage multiple priorities and work effectively in a collaborative team environment.\n\n#J-18808-Ljbffr","datePosted":"2026-09-23T04:29:42.575Z","dateModified":"2026-09-23T04:29:42.575Z","hiringOrganization":{"@type":"Organization","name":"Ultimate Staffing","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Irvine","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"1d2c258cadeaccf349a4cd09"},"url":"https://jobsearcher.com/jobs/1d2c258cadeaccf349a4cd09"}}