{"schemaVersion":"jobsearcher.job.v1","id":"fc76ea01d4ebcb8c02f3c9a1","url":"https://jobsearcher.com/jobs/fc76ea01d4ebcb8c02f3c9a1","canonicalUrl":"https://jobsearcher.com/jobs/fc76ea01d4ebcb8c02f3c9a1","title":"Contractor - Senior statistical programmer - Remote","description":"This is a Contractor - Senior statistical programmer - Remote position in a pharmaceutical company. This position will play a key role in the development, validation, and maintenance of clinical trial data analyses. This position ensures compliance with CDISC standards, adherence to regulatory requirements, and efficient execution of statistical programming deliverables. The role involves developing and validating datasets, tables, listings, and figures (TLFs) to support drug development and regulatory submissions for multiple indications.Key ResponsibilitiesPreference for candidates in EST or a similar time zone5–10 years of clinical trial programming experienceStrong Phase2/Phase3 experience, with an emphasis on ADaM dataset programming and TFL developmentStrong SDTM experience is preferred but not requiredAbility to work independently, including programming without detailed data specificationsExperience supporting internal data requests and working in a fast-paced, growing environmentAbility to prioritize urgent requests and multitask effectivelyAsthma experience is a plus but not requiredSubmission experience is also a plusExperience with R and/or Python is a nice-to-havePreference for candidates who have worked within a small-to-midsize sponsor environmentQualificationsBachelor’s or Master’s degree in Statistics, Computer Science, or a related field.Minimum 5 years of relevant experience in the biopharmaceutical, biotechnology, or CRO industry.Experience in late-phase (phase III) trials is highly desirable.Proficiency in SAS programming.Hands-on experience with raw datasets, SDTM, and ADaM dataset development.Strong analytical, problem-solving, and communication skills (both verbal and written).Ability to work effectively in a cross-functional environment, proactively influencing teams with innovative clinical development strategies.","company":"Datawise","rawCompany":"datawise","city":"Springfield","state":"MA","isRemote":true,"isActive":false,"createdAt":"2026-10-08T03:23:34.033Z","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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Contractor - Senior statistical programmer - Remote","description":"This is a Contractor - Senior statistical programmer - Remote position in a pharmaceutical company. This position will play a key role in the development, validation, and maintenance of clinical trial data analyses. This position ensures compliance with CDISC standards, adherence to regulatory requirements, and efficient execution of statistical programming deliverables. The role involves developing and validating datasets, tables, listings, and figures (TLFs) to support drug development and regulatory submissions for multiple indications.Key ResponsibilitiesPreference for candidates in EST or a similar time zone5–10 years of clinical trial programming experienceStrong Phase2/Phase3 experience, with an emphasis on ADaM dataset programming and TFL developmentStrong SDTM experience is preferred but not requiredAbility to work independently, including programming without detailed data specificationsExperience supporting internal data requests and working in a fast-paced, growing environmentAbility to prioritize urgent requests and multitask effectivelyAsthma experience is a plus but not requiredSubmission experience is also a plusExperience with R and/or Python is a nice-to-havePreference for candidates who have worked within a small-to-midsize sponsor environmentQualificationsBachelor’s or Master’s degree in Statistics, Computer Science, or a related field.Minimum 5 years of relevant experience in the biopharmaceutical, biotechnology, or CRO industry.Experience in late-phase (phase III) trials is highly desirable.Proficiency in SAS programming.Hands-on experience with raw datasets, SDTM, and ADaM dataset development.Strong analytical, problem-solving, and communication skills (both verbal and written).Ability to work effectively in a cross-functional environment, proactively influencing teams with innovative clinical development strategies.","datePosted":"2026-10-08T03:23:34.033Z","dateModified":"2026-10-08T03:23:34.033Z","hiringOrganization":{"@type":"Organization","name":"Datawise","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Springfield","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fc76ea01d4ebcb8c02f3c9a1"},"url":"https://jobsearcher.com/jobs/fc76ea01d4ebcb8c02f3c9a1"}}