{"schemaVersion":"jobsearcher.job.v1","id":"48ac9247da804ae6d1d39303","url":"https://jobsearcher.com/jobs/48ac9247da804ae6d1d39303","canonicalUrl":"https://jobsearcher.com/jobs/48ac9247da804ae6d1d39303","title":"Associate Analyst, Statistical Programming","description":"About this role\r\nThe Associate 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. This position contributes to study timelines, supports implementation of data standards, and assists in resolving data and programming issues under supervision.\r\nWhat you'll do\r\n\r\nSupport coordination, delivery, and review of statistical programming outputs across assigned studies\r\nDevelop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues\r\nContribute to end-to-end programming from CRF data collection through regulatory submission\r\nSupport preparation of submission deliverables (define.xml, XPTs, reviewer documentation)\r\nCollaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance\r\nAssist with process improvement initiatives and departmental efficiency efforts\r\n\r\nWho you are\r\n\r\nDetail-oriented with ability to manage multiple priorities\r\nCollaborative and comfortable working cross-functionally\r\nAble to communicate progress, risks, and issues clearly\r\nInterested in applying statistical programming standards in a clinical environment\r\n\r\nRequired skills\r\n\r\nBachelor's degree in Statistics, Mathematics, or related field\r\n0-2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)\r\nExposure to clinical trials, data management, or statistical analysis\r\nBasic knowledge of CDISC standards and clinical data structures\r\nUnderstanding of drug development process and regulatory requirements\r\n\r\nPreferred skills\r\n\r\nMaster's or PhD in Statistics, Mathematics, or related field\r\nExperience with regulatory submissions (e.g., define.xml, SDTM/ADaM datasets)\r\nFamiliarity with R, UNIX, or other statistical programming tools\r\nKnowledge of ICH/FDA guidelines and submission standards\r\n\r\nJob Level: Professional\r\nAdditional Information\r\nThe base compensation range for this role is: $67,000.00-$87,000.00\r\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.\r\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.\r\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:\r\n\r\nMedical, Dental, Vision, & Life insurances\r\nFitness & Wellness programs including a fitness reimbursement\r\nShort- and Long-Term Disability insurance\r\nA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)\r\nUp to 12 company paid holidays + 3 paid days off for Personal Significance\r\n80 hours of sick time per calendar year\r\nPaid Maternity and Parental Leave benefit\r\n401(k) program participation with company matched contributions\r\nEmployee stock purchase plan\r\nTuition reimbursement of up to $10,000 per calendar year\r\nEmployee Resource Groups participation\r\n\r\nWhy Biogen?\r\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.\r\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 DE&I efforts.\r\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.","company":"Biogen Idec","rawCompany":"biogen idec","city":"Durham","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-06-16T07:14:00.593Z","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":"About this role\r\nThe Associate 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. This position contributes to study timelines, supports implementation of data standards, and assists in resolving data and programming issues under supervision.\r\nWhat you'll do\r\n\r\nSupport coordination, delivery, and review of statistical programming outputs across assigned studies\r\nDevelop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues\r\nContribute to end-to-end programming from CRF data collection through regulatory submission\r\nSupport preparation of submission deliverables (define.xml, XPTs, reviewer documentation)\r\nCollaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance\r\nAssist with process improvement initiatives and departmental efficiency efforts\r\n\r\nWho you are\r\n\r\nDetail-oriented with ability to manage multiple priorities\r\nCollaborative and comfortable working cross-functionally\r\nAble to communicate progress, risks, and issues clearly\r\nInterested in applying statistical programming standards in a clinical environment\r\n\r\nRequired skills\r\n\r\nBachelor's degree in Statistics, Mathematics, or related field\r\n0-2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)\r\nExposure to clinical trials, data management, or statistical analysis\r\nBasic knowledge of CDISC standards and clinical data structures\r\nUnderstanding of drug development process and regulatory requirements\r\n\r\nPreferred skills\r\n\r\nMaster's or PhD in Statistics, Mathematics, or related field\r\nExperience with regulatory submissions (e.g., define.xml, SDTM/ADaM datasets)\r\nFamiliarity with R, UNIX, or other statistical programming tools\r\nKnowledge of ICH/FDA guidelines and submission standards\r\n\r\nJob Level: Professional\r\nAdditional Information\r\nThe base compensation range for this role is: $67,000.00-$87,000.00\r\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.\r\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.\r\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:\r\n\r\nMedical, Dental, Vision, & Life insurances\r\nFitness & Wellness programs including a fitness reimbursement\r\nShort- and Long-Term Disability insurance\r\nA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)\r\nUp to 12 company paid holidays + 3 paid days off for Personal Significance\r\n80 hours of sick time per calendar year\r\nPaid Maternity and Parental Leave benefit\r\n401(k) program participation with company matched contributions\r\nEmployee stock purchase plan\r\nTuition reimbursement of up to $10,000 per calendar year\r\nEmployee Resource Groups participation\r\n\r\nWhy Biogen?\r\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.\r\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 DE&I efforts.\r\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.","datePosted":"2026-06-16T07:14:00.593Z","dateModified":"2026-06-16T07:14:00.593Z","hiringOrganization":{"@type":"Organization","name":"Biogen Idec","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"48ac9247da804ae6d1d39303"},"url":"https://jobsearcher.com/jobs/48ac9247da804ae6d1d39303"}}