{"schemaVersion":"jobsearcher.job.v1","id":"faa12eee303d3db437be7caf","url":"https://jobsearcher.com/jobs/faa12eee303d3db437be7caf","canonicalUrl":"https://jobsearcher.com/jobs/faa12eee303d3db437be7caf","title":"Data Manager","description":"Description:\n\nBASIC SUMMARY:\n\nPerform the execution of Clinical Data Management functions with delegated authority. Interactively participate in the day-to-day development of the client deliverables while providing supervision and mentorship to Data Management Interns.\n\nESSENTIAL DUTIES AND RESPONSIBILITIES:\n\nReview study-specific documentation as part of the project team to obtain understanding of study-specific data processing conventions.\nPrepare data for entry through completion of transmittal verification, data tracking, and completion of manual review processes.\nPerform data entry in any clinical data management system used by Clinical Data Management.\nReconcile project files and other documents generated in data management against a database for accuracy and completeness of data management processes.\nInvestigate and resolve data anomalies.\nIdentify the need for and generate data queries at any point during data processing, based on guidelines set forth in the Data Management Plan (DMP).\nIssue and review queries for completeness and forward to the project lead or designee.\nConduct quality control including case report form to database review processes.\nCreate test data, perform testing procedure of entry screens, and provide test results to the project lead or designee.\nWork concurrently and accurately on multiple protocols.\nExecute all coding activities involved with developing and maintaining a clinical trials database for analysis and/or transfer to sponsor.\nProvide functional oversight of data processing activities including training of staff performing data entry, data cleaning and quality control tasks.\nReport routine project status and data trends to project lead or departmental management as required.\nCreate case report forms in accordance with the protocol and established standards when necessary.\nAuthor portions of or totality of the DMP as required.\nServe as resource for project lead and departmental management.\nAssist in staffing assignments for assigned projects, ensuring that the project is sufficiently staffed with qualified personnel and specific project requirements are met.\nProvide functional management and supervision of specific projects tasks, as well as conduct timely and through evaluation of work performance of all direct report personnel.\nAssist in providing in-house instruction and mentorship as part of technical career development for Data Management Interns, including training, progress assessment, and facilitate technical development for direct report employees.\nPerform all other related duties as assigned.\nRequirements:\n\nQUALIFICATIONS:\n\nEducation: Associate’s degree (A.A./A.S.) or equivalent in a scientific, computer, or related discipline. Bachelor’s degree preferred.\nExperience: 1 year related experience in clinical data management.\nAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.\nCertification/Licensure: None.\nOther:\nExperience with relational databases and clinical data management systems\nDemonstrated knowledge of the conduct of general data management and data management quality control activities for a clinical study\nAbility to read, write, speak and understand English required.\n\nPHYSICAL DEMANDS:\n\nWhile performing the duties of this job, the employee is regularly required to talk, hear, type/work at a computer.\nSpecific vision abilities required by this job include close vision and the ability to adjust focus.\n\nWORK ENVIRONMENT:\n\nGeneral office working conditions, the noise level in the work environment is usually quiet.\n\nCOMMENTS:\n\nMust have a valid driver’s license with no limitations on driving availability.","company":"Pharpoint Research","rawCompany":"pharpoint research","city":"Durham","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-09-17T08:08:03.739Z","occupations":[{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"15-1243.01","title":"Data Warehousing Specialists","slug":"data-warehousing-specialists"},{"code":"11-9111.00","title":"Medical and Health Services Managers","slug":"medical-and-health-services-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":"Data Manager","description":"Description:\n\nBASIC SUMMARY:\n\nPerform the execution of Clinical Data Management functions with delegated authority. Interactively participate in the day-to-day development of the client deliverables while providing supervision and mentorship to Data Management Interns.\n\nESSENTIAL DUTIES AND RESPONSIBILITIES:\n\nReview study-specific documentation as part of the project team to obtain understanding of study-specific data processing conventions.\nPrepare data for entry through completion of transmittal verification, data tracking, and completion of manual review processes.\nPerform data entry in any clinical data management system used by Clinical Data Management.\nReconcile project files and other documents generated in data management against a database for accuracy and completeness of data management processes.\nInvestigate and resolve data anomalies.\nIdentify the need for and generate data queries at any point during data processing, based on guidelines set forth in the Data Management Plan (DMP).\nIssue and review queries for completeness and forward to the project lead or designee.\nConduct quality control including case report form to database review processes.\nCreate test data, perform testing procedure of entry screens, and provide test results to the project lead or designee.\nWork concurrently and accurately on multiple protocols.\nExecute all coding activities involved with developing and maintaining a clinical trials database for analysis and/or transfer to sponsor.\nProvide functional oversight of data processing activities including training of staff performing data entry, data cleaning and quality control tasks.\nReport routine project status and data trends to project lead or departmental management as required.\nCreate case report forms in accordance with the protocol and established standards when necessary.\nAuthor portions of or totality of the DMP as required.\nServe as resource for project lead and departmental management.\nAssist in staffing assignments for assigned projects, ensuring that the project is sufficiently staffed with qualified personnel and specific project requirements are met.\nProvide functional management and supervision of specific projects tasks, as well as conduct timely and through evaluation of work performance of all direct report personnel.\nAssist in providing in-house instruction and mentorship as part of technical career development for Data Management Interns, including training, progress assessment, and facilitate technical development for direct report employees.\nPerform all other related duties as assigned.\nRequirements:\n\nQUALIFICATIONS:\n\nEducation: Associate’s degree (A.A./A.S.) or equivalent in a scientific, computer, or related discipline. Bachelor’s degree preferred.\nExperience: 1 year related experience in clinical data management.\nAn equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.\nCertification/Licensure: None.\nOther:\nExperience with relational databases and clinical data management systems\nDemonstrated knowledge of the conduct of general data management and data management quality control activities for a clinical study\nAbility to read, write, speak and understand English required.\n\nPHYSICAL DEMANDS:\n\nWhile performing the duties of this job, the employee is regularly required to talk, hear, type/work at a computer.\nSpecific vision abilities required by this job include close vision and the ability to adjust focus.\n\nWORK ENVIRONMENT:\n\nGeneral office working conditions, the noise level in the work environment is usually quiet.\n\nCOMMENTS:\n\nMust have a valid driver’s license with no limitations on driving availability.","datePosted":"2026-09-17T08:08:03.739Z","dateModified":"2026-09-17T08:08:03.739Z","hiringOrganization":{"@type":"Organization","name":"Pharpoint Research","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"faa12eee303d3db437be7caf"},"url":"https://jobsearcher.com/jobs/faa12eee303d3db437be7caf"}}