{"schemaVersion":"jobsearcher.job.v1","id":"cdc014fdcdbc0d4e2866aa73","url":"https://jobsearcher.com/jobs/cdc014fdcdbc0d4e2866aa73","canonicalUrl":"https://jobsearcher.com/jobs/cdc014fdcdbc0d4e2866aa73","title":"Clinical Research Coordinator","description":"Description:\nClinical Research Coordinator (CRC)\nThe Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.\nThe CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.\nKey Responsibilities\nStudy Management & Coordination\nOrganize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.\nSupport study start-up activities including feasibility, regulatory submissions, and site activation.\nAttend investigator meetings, site initiation visits, and other study-related meetings.\nManage visit schedules and coordinate study-related activities across clinical teams.\nRecruitment, Enrollment & Consent\nCollaborate with recruitment teams to support participant screening and enrollment.\nConduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.\nEnsure protocol and regulatory requirements are met throughout the enrollment process.\nClinical Oversight & Subject Monitoring\nMonitor and assess study subjects in accordance with protocol requirements.\nIdentify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.\nEscalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.\nDocumentation, Data & Systems\nMaintain accurate and complete source documentation, case report forms, regulatory files, and study records.\nEnter study data into EDC and other required systems and manage study databases.\nComplete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.\nReport protocol deviations to the PI, sponsor, and IRB as required.\nInvestigational Product & Specimen Management\nManage investigational product accountability records and documentation.\nCollect, process, package, and ship study specimens per protocol requirements.\nPerform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.\nQuality, Compliance & Team Support\nEnsure all study activities comply with SOPs, GCP, and regulatory requirements.\nSupport quality assurance activities and audit readiness.\nProvide assistance and mentorship to fellow coordinators as needed.\nMaintain strict confidentiality of participant and study information.\nCommunication & Outreach\nServe as the primary point of contact for sponsor and CRO communications.\nParticipate in occasional outreach or community events related to clinical trials.\nEnsure timely, accurate communication of study updates and issues.\nAdditional Responsibilities\nThis job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.\nRequirements:\nKnowledge, Skills, and Abilities\nStrong leadership and communication skills\nExceptional organizational and multitasking abilities\nHigh attention to detail and commitment to regulatory compliance\nAbility to work independently and collaboratively in a multidisciplinary environment\nStrong time management and operational efficiency skills\nProficiency with office equipment and study-specific systems\nAbility to maintain strict confidentiality\nRequired Experience & Qualifications\nEducation: Bachelor’s degree in a related field\nExperience: Minimum of two (2) years of clinical research or clinical trial management experience\nPreferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)\nPhlebotomy: Prior experience performing blood draws and handling biological specimens required","company":"Tandem Intermediate","rawCompany":"tandem intermediate","city":"Eustis","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-04-14T11:06:31.997Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"}],"industries":[{"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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"621511","title":"Medical Laboratories","slug":"medical-laboratories"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Clinical Research Coordinator","description":"Description:\nClinical Research Coordinator (CRC)\nThe Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.\nThe CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.\nKey Responsibilities\nStudy Management & Coordination\nOrganize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.\nSupport study start-up activities including feasibility, regulatory submissions, and site activation.\nAttend investigator meetings, site initiation visits, and other study-related meetings.\nManage visit schedules and coordinate study-related activities across clinical teams.\nRecruitment, Enrollment & Consent\nCollaborate with recruitment teams to support participant screening and enrollment.\nConduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.\nEnsure protocol and regulatory requirements are met throughout the enrollment process.\nClinical Oversight & Subject Monitoring\nMonitor and assess study subjects in accordance with protocol requirements.\nIdentify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.\nEscalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.\nDocumentation, Data & Systems\nMaintain accurate and complete source documentation, case report forms, regulatory files, and study records.\nEnter study data into EDC and other required systems and manage study databases.\nComplete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.\nReport protocol deviations to the PI, sponsor, and IRB as required.\nInvestigational Product & Specimen Management\nManage investigational product accountability records and documentation.\nCollect, process, package, and ship study specimens per protocol requirements.\nPerform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.\nQuality, Compliance & Team Support\nEnsure all study activities comply with SOPs, GCP, and regulatory requirements.\nSupport quality assurance activities and audit readiness.\nProvide assistance and mentorship to fellow coordinators as needed.\nMaintain strict confidentiality of participant and study information.\nCommunication & Outreach\nServe as the primary point of contact for sponsor and CRO communications.\nParticipate in occasional outreach or community events related to clinical trials.\nEnsure timely, accurate communication of study updates and issues.\nAdditional Responsibilities\nThis job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.\nRequirements:\nKnowledge, Skills, and Abilities\nStrong leadership and communication skills\nExceptional organizational and multitasking abilities\nHigh attention to detail and commitment to regulatory compliance\nAbility to work independently and collaboratively in a multidisciplinary environment\nStrong time management and operational efficiency skills\nProficiency with office equipment and study-specific systems\nAbility to maintain strict confidentiality\nRequired Experience & Qualifications\nEducation: Bachelor’s degree in a related field\nExperience: Minimum of two (2) years of clinical research or clinical trial management experience\nPreferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)\nPhlebotomy: Prior experience performing blood draws and handling biological specimens required","datePosted":"2026-04-14T11:06:31.997Z","dateModified":"2026-04-14T11:06:31.997Z","hiringOrganization":{"@type":"Organization","name":"Tandem Intermediate","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Eustis","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"cdc014fdcdbc0d4e2866aa73"},"url":"https://jobsearcher.com/jobs/cdc014fdcdbc0d4e2866aa73"}}