{"schemaVersion":"jobsearcher.job.v1","id":"feec2d23da92ddee8afbedb0","url":"https://jobsearcher.com/jobs/feec2d23da92ddee8afbedb0","canonicalUrl":"https://jobsearcher.com/jobs/feec2d23da92ddee8afbedb0","title":"Analyst, Statistical Programming","description":"This is a hybrid position that requires in-person weekly workdays at our offices in Durham, NC or in Cambridge, MA\n\nAbout this role\nThe Analyst, Statistical Programming supports statistical programming activities across clinical development programs, partnering with Biostatistics, Data Management, and external vendors to deliver high-quality, submission-ready statistical outputs. This role contributes to analysis datasets, specifications, tables, listings, figures, electronic submission components, and ad hoc analyses while ensuring compliance with data and programming standards. The position also helps drive study execution, process improvement, and implementation of Biogen's data strategy.\n\nWhat you’ll do\n\nCo-lead, under supervision, the planning, coordination, oversight, review, completion, and delivery of statistical programming activities and study deliverables.\n\nAuthor and review CDISC ADaM analysis dataset specifications and identify potential data quality concerns.\n\nCollaborate with statisticians to define, document, and implement endpoint programming algorithms.\n\nManage end-to-end programming activities from CRF collection through electronic submissions, including define.xml and XPT deliverables.\n\nPartner with submission and standards teams to ensure regulatory compliance and quality.\n\nSupport continuous improvement initiatives that enhance programming processes and efficiency.\n\nServe as the Statistical Programming co-lead for assigned studies and communicate resource needs, risks, and issues.\n\nProvide oversight and quality review of vendor programming activities and deliverables.\n\nEnsure consistent implementation of analysis, data, and submission standards across studies.\n\nWho you are\nYou are a detail-oriented statistical programming professional with strong analytical and programming capabilities. You thrive in a collaborative environment, effectively manage competing priorities, and contribute to delivering high-quality clinical trial data and analyses. You embrace Biogen's culture of pioneering, thinking broadly, driving results, and fostering an ethical and inclusive workplace.\n\nRequired skills\n\nBachelor’s degree required and Masters preferred in Statistics, Mathematics, Computer Science or other related STEAM fields.\n\n2+ years’ relevant work experience within an organization with a focus on data management and analysis\n\n2+ years SAS Base programming using SAS STAT, GRAPH and MACRO\n\n2+ years relevant experience from industry, on clinical trial and clinical database.\n\nCDISC and/or submissions experience\n\nSome knowledge of drug development process and clinical trials.\n\nSome familiarity with UNIX as well as software development packages (R, Imaging and Genomics software packages)\n\nSome familiarity AI and ML concepts\n\nPreferred skills\n\nExperience working in early phase studies (phase I, first-in-human, HV etc.)\n\nExperience from PK/PD analyses (NCA, WinNonLin, PopPK, NONMEM etc.)\n\nSome knowledge of drug submission requirements, relevant ICH and FDA/EMEA/ROW guidelines.\n\nJob Level: Professional\n\nAdditional Information\nThe base compensation range for this role is: $81,000.00-$111,000.00\n\nBase salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.\n\nRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.\n\nIn addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:\n\nMedical, Dental, Vision, & Life insurances\n\nFitness & Wellness programs including a fitness reimbursement\n\nShort- and Long-Term Disability insurance\n\nA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)\n\nUp to 12 company paid holidays + 3 paid days off for Personal Significance\n\n80 hours of sick time per calendar year\n\nPaid Maternity and Parental Leave benefit\n\n401(k) program participation with company matched contributions\n\nEmployee stock purchase plan\n\nTuition reimbursement of up to $10,000 per calendar year\n\nEmployee Resource Groups participation\n\nWhy Biogen?\nWe are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.\n\nAt Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.\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":"Ncbiotech","rawCompany":"ncbiotech","city":"Raleigh","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-08-06T03:49:20.282Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2051.00","title":"Data Scientists","slug":"data-scientists"}],"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":"Analyst, Statistical Programming","description":"This is a hybrid position that requires in-person weekly workdays at our offices in Durham, NC or in Cambridge, MA\n\nAbout this role\nThe Analyst, Statistical Programming supports statistical programming activities across clinical development programs, partnering with Biostatistics, Data Management, and external vendors to deliver high-quality, submission-ready statistical outputs. This role contributes to analysis datasets, specifications, tables, listings, figures, electronic submission components, and ad hoc analyses while ensuring compliance with data and programming standards. The position also helps drive study execution, process improvement, and implementation of Biogen's data strategy.\n\nWhat you’ll do\n\nCo-lead, under supervision, the planning, coordination, oversight, review, completion, and delivery of statistical programming activities and study deliverables.\n\nAuthor and review CDISC ADaM analysis dataset specifications and identify potential data quality concerns.\n\nCollaborate with statisticians to define, document, and implement endpoint programming algorithms.\n\nManage end-to-end programming activities from CRF collection through electronic submissions, including define.xml and XPT deliverables.\n\nPartner with submission and standards teams to ensure regulatory compliance and quality.\n\nSupport continuous improvement initiatives that enhance programming processes and efficiency.\n\nServe as the Statistical Programming co-lead for assigned studies and communicate resource needs, risks, and issues.\n\nProvide oversight and quality review of vendor programming activities and deliverables.\n\nEnsure consistent implementation of analysis, data, and submission standards across studies.\n\nWho you are\nYou are a detail-oriented statistical programming professional with strong analytical and programming capabilities. You thrive in a collaborative environment, effectively manage competing priorities, and contribute to delivering high-quality clinical trial data and analyses. You embrace Biogen's culture of pioneering, thinking broadly, driving results, and fostering an ethical and inclusive workplace.\n\nRequired skills\n\nBachelor’s degree required and Masters preferred in Statistics, Mathematics, Computer Science or other related STEAM fields.\n\n2+ years’ relevant work experience within an organization with a focus on data management and analysis\n\n2+ years SAS Base programming using SAS STAT, GRAPH and MACRO\n\n2+ years relevant experience from industry, on clinical trial and clinical database.\n\nCDISC and/or submissions experience\n\nSome knowledge of drug development process and clinical trials.\n\nSome familiarity with UNIX as well as software development packages (R, Imaging and Genomics software packages)\n\nSome familiarity AI and ML concepts\n\nPreferred skills\n\nExperience working in early phase studies (phase I, first-in-human, HV etc.)\n\nExperience from PK/PD analyses (NCA, WinNonLin, PopPK, NONMEM etc.)\n\nSome knowledge of drug submission requirements, relevant ICH and FDA/EMEA/ROW guidelines.\n\nJob Level: Professional\n\nAdditional Information\nThe base compensation range for this role is: $81,000.00-$111,000.00\n\nBase salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.\n\nRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.\n\nIn addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:\n\nMedical, Dental, Vision, & Life insurances\n\nFitness & Wellness programs including a fitness reimbursement\n\nShort- and Long-Term Disability insurance\n\nA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)\n\nUp to 12 company paid holidays + 3 paid days off for Personal Significance\n\n80 hours of sick time per calendar year\n\nPaid Maternity and Parental Leave benefit\n\n401(k) program participation with company matched contributions\n\nEmployee stock purchase plan\n\nTuition reimbursement of up to $10,000 per calendar year\n\nEmployee Resource Groups participation\n\nWhy Biogen?\nWe are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.\n\nAt Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.\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":"2026-08-06T03:49:20.282Z","dateModified":"2026-08-06T03:49:20.282Z","hiringOrganization":{"@type":"Organization","name":"Ncbiotech","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Raleigh","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"feec2d23da92ddee8afbedb0"},"url":"https://jobsearcher.com/jobs/feec2d23da92ddee8afbedb0"}}