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Clinical research, Oncology, inpatient, Gcp, Irb, Data management, BLS, CPR, AED, Registered Nurse, communication and leadership skills, CCRC or CCRP Certified, patient registration, quality assurance, subject eligibility, EMR, clinical trial, regulatory, oncology nursing, chart review, enrollment, adverse event reporting.
$30 - $45 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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ResponsibilitiesA day in the life of a Clinical Research Nurse at Hackensack Meridian Health includes:Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
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Odyssey is seeking a Registered Nurse (RN) for a Clinical Research Nurse Coordinator position to support the Clinical Investigation Department (CID) in the Cancer Coordination Center at the Navy Medical Center, Portsmouth (NMCP) Virginia.
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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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The Medical Faculty Associates is looking for a clinical research nurse to join the Division of Infectious Diseases (ID) with responsibilities in clinical research operations.
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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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Overview The Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of cancer as a disease process, cancer treatment modalities (or comparable knowledge for a non-oncology area, e.g. infection control) and the process of conducting medical clinical research.
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The Clinical Research Nurse will be able to function as a Clinical Research Coordinator and shall assist primary investigators with the following tasks in order to develop institutionally.
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Study Coordinator, Clinical Research Coordinator, Clinical Research Regulatory. Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health delivery systems in California, seeks an accomplished Clinical Research Coordinator.
$30 - $35 an hourExpandApply NowActive JobUpdated 20 days ago - 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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Understanding of basic anatomy and physiology, electrophysiology and arrhythmiasRegistered Nurse with previous clinical research experience as either a CRA or Study Coordinator. POSITION SUMMARY:The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, includingclinical monitoring of AtriCure also includes the coordination of site activities from site start-up to site closure as needed.
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Clinical Research Associate II Cincinnati, OH, USA ● Mason, OH, USA ● Minneapolis, MN, USA ● Minnetonka, MN, USA Req #1992 Friday, March 22, 2024 AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions.
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The Senior Clinical Research Associate (Sr. CRA) is an integral member of the clinical study team, effectively managing multiple priorities to ensure study subject safety, and successful data collection and integrity of the clinical trial.
$138,500 - $153,100 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Job Req ID: 112971 Clinical Research Monitor The Department of Neurology is seeking a who will take the lead on compliance monitoring of predominantly large, multi-centered, clinical trials in keeping with established BIOS Clinical Trials Coordinating Center (CTCC) policies and procedures and GCP. The CRM will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials through utilization of a risk-based, remote monitoring approach.
$55,200 - $96,600 a year depends on experienceFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 14 days ago
Title: clinical research nurse Company: University Of Minnesota University Services Human Resources
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