{"schemaVersion":"jobsearcher.job.v1","id":"5d552eb1189698a9d843ca1e","url":"https://jobsearcher.com/jobs/5d552eb1189698a9d843ca1e","canonicalUrl":"https://jobsearcher.com/jobs/5d552eb1189698a9d843ca1e","title":"Data Coordinator","description":"Overview\nIn this role, you support the Study Coordinator to drive clinical trial data integrity within SCRI’s drug development operations. You help ensure SOP, GCP, and ICH compliance while handling source data, CRF completion, and SAE activities. You will contribute to efficient trial management, patient tracking, and archival of study files. This is a mission-driven position at a leading oncology research organization with meaningful patient impact.\n\nCompensation / BenefitsTotal Rewards package with comprehensive benefitsCompetitive compensationAnnual bonus or long-term incentive opportunitiesSupport for physical, mental, and financial well-beingMcKesson-related benefits access\nResponsibilitiesSupport the Study Coordinator to meet trial data deadlinesObtain source documentation for enrolled patientsAssist in case report form completion and query resolutionAssist in SAE reporting and trackingCreate and maintain patient visit tracking spreadsheetsMaintain and archive study administrative filesUndertake procedural projects to improve Drug Development Data OperationsAssess adherence to SCRI SOPs, GCP and ICH regulations during the trial\nKey requirementsKnowledge of scientific, medical, and regulatory termsKnowledge of GCP and GMPDetail-orientedExcellent English written and oral skillsBachelor Degree preferredHealthcare experience, clinical trials support, or pharmaceutical industry experience preferredDetail-orientedStrong written and verbal communication in EnglishCollaborative with cross-functional teamsGCP and GMP knowledgeRegulatory terminology熟悉Clinical trial data management familiarity","company":"McKesson","rawCompany":"mckesson","city":"Winter Park","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-09-15T03:37:01.372Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"43-9021.00","title":"Data Entry Keyers","slug":"data-entry-keyers"}],"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":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Data Coordinator","description":"Overview\nIn this role, you support the Study Coordinator to drive clinical trial data integrity within SCRI’s drug development operations. You help ensure SOP, GCP, and ICH compliance while handling source data, CRF completion, and SAE activities. You will contribute to efficient trial management, patient tracking, and archival of study files. This is a mission-driven position at a leading oncology research organization with meaningful patient impact.\n\nCompensation / BenefitsTotal Rewards package with comprehensive benefitsCompetitive compensationAnnual bonus or long-term incentive opportunitiesSupport for physical, mental, and financial well-beingMcKesson-related benefits access\nResponsibilitiesSupport the Study Coordinator to meet trial data deadlinesObtain source documentation for enrolled patientsAssist in case report form completion and query resolutionAssist in SAE reporting and trackingCreate and maintain patient visit tracking spreadsheetsMaintain and archive study administrative filesUndertake procedural projects to improve Drug Development Data OperationsAssess adherence to SCRI SOPs, GCP and ICH regulations during the trial\nKey requirementsKnowledge of scientific, medical, and regulatory termsKnowledge of GCP and GMPDetail-orientedExcellent English written and oral skillsBachelor Degree preferredHealthcare experience, clinical trials support, or pharmaceutical industry experience preferredDetail-orientedStrong written and verbal communication in EnglishCollaborative with cross-functional teamsGCP and GMP knowledgeRegulatory terminology熟悉Clinical trial data management familiarity","datePosted":"2026-09-15T03:37:01.372Z","dateModified":"2026-09-15T03:37:01.372Z","hiringOrganization":{"@type":"Organization","name":"McKesson","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Winter Park","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"5d552eb1189698a9d843ca1e"},"url":"https://jobsearcher.com/jobs/5d552eb1189698a9d843ca1e"}}