{"schemaVersion":"jobsearcher.job.v1","id":"d73bc975a8964967d4b1f917","url":"https://jobsearcher.com/jobs/d73bc975a8964967d4b1f917","canonicalUrl":"https://jobsearcher.com/jobs/d73bc975a8964967d4b1f917","title":"Database Programmer - WFH","description":"## About the RoleGQR's client is seeking a Senior Clinical Database Programmer with hands-on Veeva CDMS experience to support oncology clinical trials. This role focuses on building and maintaining high-quality clinical study databases, configuring EDC components, supporting user acceptance testing, and helping drive database development through go-live.The position partners closely with Lead Data Managers and study teams and requires strong ownership, attention to quality, and experience working across clinical trial data workflows.## Key Responsibilities* Build and maintain study databases in Veeva CDMS according to study protocols and specifications.* Configure forms, visit schedules, edit checks/rules, and derivations.* Lead database development timelines and quality checkpoints.* Plan, execute, and support UAT activities.* Resolve UAT issues and coordinate required approvals.* Support integrations including ePRO, IWRS, and laboratory systems.* Coordinate technical details related to clinical data integrations.* Provide best-practice guidance to study teams.* Create and maintain relevant documentation.* Provide training and support to study teams.* Manage responsibilities across multiple studies while maintaining strong ownership and follow-through.## Required Qualifications* 2+ years of end-to-end experience with Veeva CDMS or Veeva EDC.* 5+ years of experience in clinical trial operations or clinical data workflows within pharmaceutical or biotechnology environments.* Strong knowledge of CRF design standards.* Strong knowledge of edit check design standards and documentation.* Experience supporting multiple clinical studies simultaneously.* Experience with oncology clinical trials and/or global Phase I–III trials.* Familiarity with CDISC, CDASH, and SDTM.* Experience with EDC integrations.## Work Arrangement* Remote position within the United States.* Must be available to support core Pacific / West Coast hours.* 18-month contract.* Mid-Senior level.* Science-focused role within biotechnology research and pharmaceutical manufacturing.## Compensation & Benefits* Pay: Low-to-mid $90s per hour, depending on experience.* Medical insurance.* Vision insurance.* 401(k).* Disability insurance.Apply Now","company":"Torentify","rawCompany":"torentify","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-10-01T22:54:52.160Z","occupations":[{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"15-1252.00","title":"Software Developers","slug":"software-developers"},{"code":"15-1251.00","title":"Computer Programmers","slug":"computer-programmers"}],"industries":[{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"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":"Database Programmer - WFH","description":"## About the RoleGQR's client is seeking a Senior Clinical Database Programmer with hands-on Veeva CDMS experience to support oncology clinical trials. This role focuses on building and maintaining high-quality clinical study databases, configuring EDC components, supporting user acceptance testing, and helping drive database development through go-live.The position partners closely with Lead Data Managers and study teams and requires strong ownership, attention to quality, and experience working across clinical trial data workflows.## Key Responsibilities* Build and maintain study databases in Veeva CDMS according to study protocols and specifications.* Configure forms, visit schedules, edit checks/rules, and derivations.* Lead database development timelines and quality checkpoints.* Plan, execute, and support UAT activities.* Resolve UAT issues and coordinate required approvals.* Support integrations including ePRO, IWRS, and laboratory systems.* Coordinate technical details related to clinical data integrations.* Provide best-practice guidance to study teams.* Create and maintain relevant documentation.* Provide training and support to study teams.* Manage responsibilities across multiple studies while maintaining strong ownership and follow-through.## Required Qualifications* 2+ years of end-to-end experience with Veeva CDMS or Veeva EDC.* 5+ years of experience in clinical trial operations or clinical data workflows within pharmaceutical or biotechnology environments.* Strong knowledge of CRF design standards.* Strong knowledge of edit check design standards and documentation.* Experience supporting multiple clinical studies simultaneously.* Experience with oncology clinical trials and/or global Phase I–III trials.* Familiarity with CDISC, CDASH, and SDTM.* Experience with EDC integrations.## Work Arrangement* Remote position within the United States.* Must be available to support core Pacific / West Coast hours.* 18-month contract.* Mid-Senior level.* Science-focused role within biotechnology research and pharmaceutical manufacturing.## Compensation & Benefits* Pay: Low-to-mid $90s per hour, depending on experience.* Medical insurance.* Vision insurance.* 401(k).* Disability insurance.Apply Now","datePosted":"2026-10-01T22:54:52.160Z","dateModified":"2026-10-01T22:54:52.160Z","hiringOrganization":{"@type":"Organization","name":"Torentify","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d73bc975a8964967d4b1f917"},"url":"https://jobsearcher.com/jobs/d73bc975a8964967d4b1f917"}}