{"schemaVersion":"jobsearcher.job.v1","id":"3b3046c9e2be2efd70275db4","url":"https://jobsearcher.com/jobs/3b3046c9e2be2efd70275db4","canonicalUrl":"https://jobsearcher.com/jobs/3b3046c9e2be2efd70275db4","title":"Statistical Programming Contractor","description":"Position Summary:\n\nThe Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates closely with Biostatistics and other cross-functional team members to produce high-quality, compliant datasets, tables, listings, and figures while ensuring adherence to project timelines, SOPs, regulatory requirements, and CDISC standards.\n\nResponsibilities:\n\nProgram and validate tables, listings, figures, and derived datasets using SAS.\nDevelop SDTM and ADaM specs, datasets, and supporting documentation.\nPrepare and review mapping specifications, annotated case report forms (aCRF), define, SDRG, ADRG and other files needed in the submission.\nPerform quality control and validation activities for all programming deliverables.\nCollaborate with study team members to identify, investigate, and resolve data and output issues.\nReview study documents and provide input to improve programming quality, efficiency, and consistency.\nMaintain complete, accurate, and audit-/inspection-ready programming documentation.\nCommunicate project status, risks, issues, and timeline impacts clearly to stakeholders.\nOther as assigned.\n\n Qualifications:\n\nBachelor’s degree required; Master’s degree preferred in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.\nMinimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.\nPhase 3 and regulatory submission experience preferred.\nStrong SAS programming skills, with experience developing SDTM, ADaM, tables, listings, and figures.\nStrong knowledge of clinical trial processes, regulatory requirements, and programming documentation.\nHigh attention to detail, with strong analytical, problem-solving, and communication skills.\nAbility to work independently and manage multiple priorities in a deadline-driven environment.\n\nProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.\n\nApplicants must be eligible to work in the United States without the need for work visa or residency sponsorship.","company":"Prokidney","rawCompany":"prokidney","city":"Myrtle Point","state":"OR","isRemote":false,"isActive":false,"createdAt":"2026-09-28T11:24:19.653Z","occupations":[{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"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":"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"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Statistical Programming Contractor","description":"Position Summary:\n\nThe Statistical Programmer Contractor is responsible for developing, validating, and maintaining SAS programming deliverables to support clinical study analysis and reporting. This role collaborates closely with Biostatistics and other cross-functional team members to produce high-quality, compliant datasets, tables, listings, and figures while ensuring adherence to project timelines, SOPs, regulatory requirements, and CDISC standards.\n\nResponsibilities:\n\nProgram and validate tables, listings, figures, and derived datasets using SAS.\nDevelop SDTM and ADaM specs, datasets, and supporting documentation.\nPrepare and review mapping specifications, annotated case report forms (aCRF), define, SDRG, ADRG and other files needed in the submission.\nPerform quality control and validation activities for all programming deliverables.\nCollaborate with study team members to identify, investigate, and resolve data and output issues.\nReview study documents and provide input to improve programming quality, efficiency, and consistency.\nMaintain complete, accurate, and audit-/inspection-ready programming documentation.\nCommunicate project status, risks, issues, and timeline impacts clearly to stakeholders.\nOther as assigned.\n\n Qualifications:\n\nBachelor’s degree required; Master’s degree preferred in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.\nMinimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.\nPhase 3 and regulatory submission experience preferred.\nStrong SAS programming skills, with experience developing SDTM, ADaM, tables, listings, and figures.\nStrong knowledge of clinical trial processes, regulatory requirements, and programming documentation.\nHigh attention to detail, with strong analytical, problem-solving, and communication skills.\nAbility to work independently and manage multiple priorities in a deadline-driven environment.\n\nProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.\n\nApplicants must be eligible to work in the United States without the need for work visa or residency sponsorship.","datePosted":"2026-09-28T11:24:19.653Z","dateModified":"2026-09-28T11:24:19.653Z","hiringOrganization":{"@type":"Organization","name":"Prokidney","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Myrtle Point","addressRegion":"OR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3b3046c9e2be2efd70275db4"},"url":"https://jobsearcher.com/jobs/3b3046c9e2be2efd70275db4"}}