{"schemaVersion":"jobsearcher.job.v1","id":"3ee3003fbbed32e85151d521","url":"https://jobsearcher.com/jobs/3ee3003fbbed32e85151d521","canonicalUrl":"https://jobsearcher.com/jobs/3ee3003fbbed32e85151d521","title":"Clinical Data Manager","description":"OverviewIn this remote, contract role you will lead clinical data management activities to ensure accurate, compliant data for analysis. You'll partner with CROs and cross-functional teams to uphold data quality and regulatory standards. Your work drives reliable datasets for meaningful patient-focused research in rare diseases and pharma. This position offers scale, impact, and collaboration within a specialized clinical data function.ResponsibilitiesServe as the primary data management contact for assigned studies and coordinate with CROsLead CDM activities aligned with company SOPs and regulatory requirementsOversee CRO data cleanup from study start-up to archiving to ensure quality and integrityManage medical coding, data validation checks, database snapshots, and provision of data for analysisCreate and maintain study documentation (Data Management Manual, CRF guidelines, validation specs)Design/modify CRFs and oversee build, test, and validation of clinical databasesPrepare and distribute project status reports to teams and managementLead the CDM team to ensure validated databases ready for transfer and analysis; support outsourcing partner process standardizationKey requirementsBachelor's degree in mathematics, science, or related fieldExperience in clinical data management within biotechnology, pharmaceuticals, or health-related industryStrong ability to coordinate and manage CRO data managers and project teamsSolid understanding of data management processes, database validation, and regulatory complianceExcellent collaboration, organizational, and communication skillsPreferred experience in genetics, oncology, and/or ophthalmologycollaborationorganizational skillsclear communicationclinical data managementdatabase validationregulatory compliance","company":"Proclinical","rawCompany":"proclinical","city":"Washington","state":"DC","isRemote":false,"isActive":false,"createdAt":"2026-10-26T14:33:12.498Z","occupations":[{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"11-9111.00","title":"Medical and Health Services Managers","slug":"medical-and-health-services-managers"}],"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":"Clinical Data Manager","description":"OverviewIn this remote, contract role you will lead clinical data management activities to ensure accurate, compliant data for analysis. You'll partner with CROs and cross-functional teams to uphold data quality and regulatory standards. Your work drives reliable datasets for meaningful patient-focused research in rare diseases and pharma. This position offers scale, impact, and collaboration within a specialized clinical data function.ResponsibilitiesServe as the primary data management contact for assigned studies and coordinate with CROsLead CDM activities aligned with company SOPs and regulatory requirementsOversee CRO data cleanup from study start-up to archiving to ensure quality and integrityManage medical coding, data validation checks, database snapshots, and provision of data for analysisCreate and maintain study documentation (Data Management Manual, CRF guidelines, validation specs)Design/modify CRFs and oversee build, test, and validation of clinical databasesPrepare and distribute project status reports to teams and managementLead the CDM team to ensure validated databases ready for transfer and analysis; support outsourcing partner process standardizationKey requirementsBachelor's degree in mathematics, science, or related fieldExperience in clinical data management within biotechnology, pharmaceuticals, or health-related industryStrong ability to coordinate and manage CRO data managers and project teamsSolid understanding of data management processes, database validation, and regulatory complianceExcellent collaboration, organizational, and communication skillsPreferred experience in genetics, oncology, and/or ophthalmologycollaborationorganizational skillsclear communicationclinical data managementdatabase validationregulatory compliance","datePosted":"2026-10-26T14:33:12.498Z","dateModified":"2026-10-26T14:33:12.498Z","hiringOrganization":{"@type":"Organization","name":"Proclinical","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Washington","addressRegion":"DC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3ee3003fbbed32e85151d521"},"url":"https://jobsearcher.com/jobs/3ee3003fbbed32e85151d521"}}