{"schemaVersion":"jobsearcher.job.v1","id":"90b50b67d00a61cfc1d54449","url":"https://jobsearcher.com/jobs/90b50b67d00a61cfc1d54449","canonicalUrl":"https://jobsearcher.com/jobs/90b50b67d00a61cfc1d54449","title":"Principal Statistical Programmer","description":"*Remote Position*Principal Statistical ProgrammerDescriptionA Principal Statistical Programmer serves as a technical resource for the department, provides programming support and management to multiple clinical trials, and is responsible for the day-to-day management of project activities and deliveries, and ensuring that the deliverables are produced with high levels of quality.Responsibilities Leads and supports statistical programming activities for clinical studies, submissions, and development initiatives. Contributes to and manages timelines and work product required to deliver high quality statistical programming services. Develops programming efficiencies to ensure a productive work environment producing deliverables of high quality. Mentors junior statistical programmers in programming methodologies and relevant company SOPs. Lead aspects of the statistical programming including:Contributes to the electronic submission of clinical trial data to regulatory authoritiesAnnotates Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines.Develops SDTM specifications and generates SDTM datasets using SAS.Develops ADaM,specifications and generates ADaM datasets using SAS based on Statistical Analysis Plan.Develops Tables, Listings, Graphs, and Patient Profiles in support of the Clinical Study Report, Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE), Posters, and Manuscripts.Creates electronic submission package to FDA, e.g., define.xml or define.pdf following FDA guidelines.Reviews draft and final production deliverables for project to ensure quality and consistency.Qualifications Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, or related scientific disciplines that provides computer literacy and numeracy, and 6 years of clinical programming experience Expert level SAS programming skills including SQL and macro development. Expert level knowledge and application of CDISC standards for SDTM and ADaM. A successful history of cross-functional collaboration. Excellent verbal and written communication skills. Excellent planning and organizational skills with the ability to adapt and adjust to changing priorities. Ability to be productive and handle multiple tasks to meet deadlines in a dynamic, fast-paced environment.Please submit your application (resume, cover letter) to HR@DuBuResearch.comQuick Apply","company":"Dubu Research","rawCompany":"dubu research","city":"Crown Point","state":"NY","isRemote":false,"isActive":false,"createdAt":"2026-07-21T10:33:12.897Z","occupations":[{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Principal Statistical Programmer","description":"*Remote Position*Principal Statistical ProgrammerDescriptionA Principal Statistical Programmer serves as a technical resource for the department, provides programming support and management to multiple clinical trials, and is responsible for the day-to-day management of project activities and deliveries, and ensuring that the deliverables are produced with high levels of quality.Responsibilities Leads and supports statistical programming activities for clinical studies, submissions, and development initiatives. Contributes to and manages timelines and work product required to deliver high quality statistical programming services. Develops programming efficiencies to ensure a productive work environment producing deliverables of high quality. Mentors junior statistical programmers in programming methodologies and relevant company SOPs. Lead aspects of the statistical programming including:Contributes to the electronic submission of clinical trial data to regulatory authoritiesAnnotates Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines.Develops SDTM specifications and generates SDTM datasets using SAS.Develops ADaM,specifications and generates ADaM datasets using SAS based on Statistical Analysis Plan.Develops Tables, Listings, Graphs, and Patient Profiles in support of the Clinical Study Report, Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE), Posters, and Manuscripts.Creates electronic submission package to FDA, e.g., define.xml or define.pdf following FDA guidelines.Reviews draft and final production deliverables for project to ensure quality and consistency.Qualifications Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, or related scientific disciplines that provides computer literacy and numeracy, and 6 years of clinical programming experience Expert level SAS programming skills including SQL and macro development. Expert level knowledge and application of CDISC standards for SDTM and ADaM. A successful history of cross-functional collaboration. Excellent verbal and written communication skills. Excellent planning and organizational skills with the ability to adapt and adjust to changing priorities. Ability to be productive and handle multiple tasks to meet deadlines in a dynamic, fast-paced environment.Please submit your application (resume, cover letter) to HR@DuBuResearch.comQuick Apply","datePosted":"2026-07-21T10:33:12.897Z","dateModified":"2026-07-21T10:33:12.897Z","hiringOrganization":{"@type":"Organization","name":"Dubu Research","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Crown Point","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"90b50b67d00a61cfc1d54449"},"url":"https://jobsearcher.com/jobs/90b50b67d00a61cfc1d54449"}}