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Participates in the Center’s research and development projects, including all efforts related to clinical trials. Measures and analyzes proton radiation data in accordance with the Center’s mission of clinical services and clinical research.
$125,000 - $200,000 a yearFull-timeExpandUpdated 17 days ago - UpvoteDownvoteShare Job
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We seek an organized, highly motivated, full-time Clinical Research Coordinator I (CRC) to join our Dystonia Partners Research Bank team in the Department of Neurology at Massachusetts General Hospital.
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Our core team includes 4 Neurologists, with our PI, Nutan Sharma, M.D., Ph. D., 2 Research Coordinators, a Clinical Research Fellow, a Staff Assistant, and a Clinical Research Program Manager/Genetic Counselor.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandUpdated 16 days ago - UpvoteDownvoteShare Job
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Clinical Research Coordinator, Norwalk, CT. Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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Nuvance Health has a network of convenient hospital and outpatient locations — Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess Hospital, Putnam Hospital Center and Vassar Brothers Medical Center in New York. Summary: The Clinical Coordinator-Wound Care is responsible for performing assessment, discharge planning, resource utilization, program planning to meet the needs of all wound care patients.
$55 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Research Coordinator predominately functions as the key coordinating lead for the local University of Chicago SuperAging site activities related to data collection and participant visits.
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The Lab Coordinator will join Clinical Pharmacology Research Laboratory under the Division of Cardiology School of Medicine at ZSFG to conduct nicotine and tobacco related researches in human.
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Additionally, the Clinical Procurement Coordinator supports donor families, provides family care and may provide families with the option of organ and/or tissue donation. The Clinical Procurement Coordinator is responsible for response to donor referrals, donor evaluation, and donor management, coordination of organ recovery, organ preservation, and organ distribution.
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JOB SUMMARY: The Clinical Research Nursing Coordinator works collaboratively with the Principal Investigator and other research staff to support study implementation. Clinical Research Nursing Coordinator.
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Lab Coordinator - Clinical Pharmacology. The Lab Coordinator will perform advance chromatographic and mass spectrometric analysis, such as Gas Chromatography (GC), Liquid Chromatography (HPLC), Gas Chromatography-Mass Spectrometry (GCMS), Gas Chromatography-Tandem Mass Spectrometry (GC-MS/MS), and Liquid Chromatography with Tandem Mass Spectrometry (LC-MS/MS); organize experimental data and keep detailed records of experiments; prepare and present reports independently.
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Today, our team continues to expand across the globe, with over 350 employees across the US, Europe, Australia, and Asia. The Role:Ora's Clinical Research Coordinator I (CRC) has close relationships with the subjects who participate in our clinical trials located regionally, domestically, and at times, internationally.
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The Travel Clinical Research Coordinator will be mentored by their CRC Lead, Site Manager, Senior Manager, and other leaders within clinical operations. Based out of the Chicago, IL area, the Travel Clinical Research Coordinator primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases.
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PREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Full-time Clinical Research Coordinator, Poughkeepsie, NY.
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Title: clinical coordinator Company: California Proton Therapy Center
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