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The Research Coordinator will assist in the conduct of Clinical Trials by ensuring protocol compliance, filing adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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The Clinical Research Coordinator works independently to support the Principal Investigator by providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$52,707.2 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist the Study Director/s in preparing an event schedule documenting all critical events to occur from the final study protocol into a scheduling database such as Microsoft Planner or a related database.
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Join our team and use your skill with an organization known nationally for excellence in research Job Summary: The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$39.76 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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If errors exist, generates queries and submits them to the coordinator/data manager associated with the protocol. Leads execution & control of research data bases for trial endpointsEnsures completion of study activities per protocol including recruitmentDevelops new and/or revised research methodologiesAscertains pretreatment & eligibility requirementsAdministrationDevelop standardized templates, policies, and procedures for internal and external reporting.
$69,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols.
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Complete substance abuse referrals for the indicated level of care, such as inpatient detox, outpatient individual/group treatment, and residential treatment, per existing protocol. The Care Coordinator (CC) will work with clinic patients to coordinate the full range of physical health, behavioral health, and community-based services.
$67,667 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Position Focus: Within the Department of Neurology’s Clinical Research Office and reporting to the Research manager with a focus on neuromuscular, the Clinical Research Coordinator (CRC) will lead efforts in the execution of research studies within the scope of the established study protocol(s) assigned.
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Request and upload radiological images into sponsor-provided imaging platforms according to each study protocol. RequirementsJob OverviewThe Research Data Coordinator 2 position is responsible for data management for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center (LCCC.
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Minimum Experience:Must be a CNA, MA, or EMT at the time of hire or be a HUC I, PCA, CNA, MA, or EMT with six or more (6+) months of experience at a Covenant Health facility and complete the Covenant Health’s Patient Care Assistant training protocol.
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Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable.
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Working skill in the use of a personal computer, utilizing word processing, spreadsheet, database, mapping and routing, and web-based route posting; accident protocol and reporting procedures. Successful completion of state-approved school bus driver training course.
$69,929 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The IGM Clinical Research coordinator’s primary responsibility is managing key elements of clinical research studies to meet protocol obligations. Conducts clinical research studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout study; adheres to good clinical practices.
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Coordinates disbursement of and administers protocol provided drug therapy. Ensures accurate research intervention (drug, device) by communication of dose modifications and protocol requirements to the physician investigator.
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
$58 an hourExpandApply NowActive JobUpdated 7 days ago
protocol job Title: coordinator
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