{"schemaVersion":"jobsearcher.job.v1","id":"8667e57f8a0013fd4f8a6f27","url":"https://jobsearcher.com/jobs/8667e57f8a0013fd4f8a6f27","canonicalUrl":"https://jobsearcher.com/jobs/8667e57f8a0013fd4f8a6f27","title":"Associate Analyst, Statistical Programming","description":"Overview\nAssociate Analyst, Statistical Programming supports statistical programming activities across clinical studies, including analysis datasets, tables, listings, figures, and regulatory submission deliverables. The role partners with Biostatistics and Data Management to produce high‑quality, submission‑ready outputs and contributes to study timelines by supporting data standards implementation and resolving programming issues under supervision.\n\nResponsibilities\n\nSupport coordination, delivery, and review of statistical programming outputs across assigned studies\n\nDevelop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues\n\nContribute to end‑to‑end programming from CRF data collection through regulatory submission\n\nSupport preparation of submission deliverables (define.xml, XPTs, reviewer documentation)\n\nCollaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance\n\nAssist with process improvement initiatives and departmental efficiency efforts\n\nQualifications\n\nDetail‑oriented with ability to manage multiple priorities\n\nCollaborative and comfortable working cross‑functionally\n\nAble to communicate progress, risks, and issues clearly\n\nInterested in applying statistical programming standards in a clinical environment\n\nRequired Skills\n\nBachelor’s degree in Statistics, Mathematics, or related field\n\n0–2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)\n\nExposure to clinical trials, data management, or statistical analysis\n\nBasic knowledge of CDISC standards and clinical data structures\n\nUnderstanding of drug development process and regulatory requirements\n\nPreferred Skills\n\nMaster’s or PhD in Statistics, Mathematics, or related field\n\nExperience with regulatory submissions (define.xml, SDTM/ADaM datasets)\n\nFamiliarity with R, UNIX, or other statistical programming tools\n\nKnowledge of ICH/FDA guidelines and submission standards\n\nBenefits\n\nMedical, Dental, Vision, & Life insurance\n\nFitness & Wellness programs including a fitness reimbursement\n\nShort‑and Long‑Term Disability insurance\n\nPaid vacation and holiday time off\n\nPaid Maternity and Parental Leave benefit\n\n401(k) program with company match\n\nEmployee stock purchase plan\n\nTuition reimbursement up to $10,000 per year\n\nAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E‑Verify Employer in the United States.\n\n#J-18808-Ljbffr","company":"Biogen","rawCompany":"biogen","city":"South Milwaukee","state":"WI","isRemote":false,"isActive":false,"createdAt":"2026-06-20T04:38:56.238Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"43-9111.00","title":"Statistical Assistants","slug":"statistical-assistants"}],"industries":[{"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"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Associate Analyst, Statistical Programming","description":"Overview\nAssociate Analyst, Statistical Programming supports statistical programming activities across clinical studies, including analysis datasets, tables, listings, figures, and regulatory submission deliverables. The role partners with Biostatistics and Data Management to produce high‑quality, submission‑ready outputs and contributes to study timelines by supporting data standards implementation and resolving programming issues under supervision.\n\nResponsibilities\n\nSupport coordination, delivery, and review of statistical programming outputs across assigned studies\n\nDevelop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues\n\nContribute to end‑to‑end programming from CRF data collection through regulatory submission\n\nSupport preparation of submission deliverables (define.xml, XPTs, reviewer documentation)\n\nCollaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance\n\nAssist with process improvement initiatives and departmental efficiency efforts\n\nQualifications\n\nDetail‑oriented with ability to manage multiple priorities\n\nCollaborative and comfortable working cross‑functionally\n\nAble to communicate progress, risks, and issues clearly\n\nInterested in applying statistical programming standards in a clinical environment\n\nRequired Skills\n\nBachelor’s degree in Statistics, Mathematics, or related field\n\n0–2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)\n\nExposure to clinical trials, data management, or statistical analysis\n\nBasic knowledge of CDISC standards and clinical data structures\n\nUnderstanding of drug development process and regulatory requirements\n\nPreferred Skills\n\nMaster’s or PhD in Statistics, Mathematics, or related field\n\nExperience with regulatory submissions (define.xml, SDTM/ADaM datasets)\n\nFamiliarity with R, UNIX, or other statistical programming tools\n\nKnowledge of ICH/FDA guidelines and submission standards\n\nBenefits\n\nMedical, Dental, Vision, & Life insurance\n\nFitness & Wellness programs including a fitness reimbursement\n\nShort‑and Long‑Term Disability insurance\n\nPaid vacation and holiday time off\n\nPaid Maternity and Parental Leave benefit\n\n401(k) program with company match\n\nEmployee stock purchase plan\n\nTuition reimbursement up to $10,000 per year\n\nAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E‑Verify Employer in the United States.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T04:38:56.238Z","dateModified":"2026-06-20T04:38:56.238Z","hiringOrganization":{"@type":"Organization","name":"Biogen","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"South Milwaukee","addressRegion":"WI","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"8667e57f8a0013fd4f8a6f27"},"url":"https://jobsearcher.com/jobs/8667e57f8a0013fd4f8a6f27"}}