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Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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The Clinical Research Coordinator will work on cutting-edge NIH and foundation founded clinical trials focusing, broadly, on mind-body resiliency research, cancer survivorship, coping with cardiovascular illness, and tobacco treatment.
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Under the direction of the Principal Investigator (PI) and Cardiology Research Nurse Manager, collaborate with all members of the clinical research team to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and that ethical obligations are kept.
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Medical Center: UH: Clinical Lab- (Full-Time, Evening Shift) - Job Summary: The Clinical Lab Scientist 1, under general supervision, operates specialized instruments to conduct clinical lab tests and analyze data from results, to assist physicians with diagnosing medical conditions.
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As one of the primary resources for the protocol, the Clinical Research Coordinator I acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator I assists with all data and source documentation, adverse event reporting and maintenance of complete regulatory files, also as a part of the learning experience.
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Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) through the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA.
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The Pediatric Solid Tumor Program at Dana-Farber Cancer Institute is seeking to hire a motivated Clinical Research Coordinator (CRC) to work within the Clinical Translational Research Program (CTIP) on trials specific to the Solid Tumor Biology and research portfolio.
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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, including clinical 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 Nurse serves as an expert oncology clinician and patient/client advocate. The Clinical Research Nurse assists the Principal Investigators (PI’s) and other participating physicians and investigators in the initial identification and evaluation of protocols to be submitted to IRB/CIRB for approval.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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This position will report directly to the Program Manager and work directly with Physician Investigators ("PI") on clinical research performed. The Clinical Research Coordinator (CRC) is an integral and essential member of the ACC CRU Melanoma Research Team. We are looking for an enthusiastic, professional and committed team member to work closely with our clinical research investigators, Research Team Leaders, our clinical research nurse(s), and regulatory coordinator.
$43,919 - $67,046 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), Certified IRB Professional (CIP), Certified IRB Manager (CIM) or Certified Clinical Research Associate (CCRA) preferred.
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This position is part of Clinical Affairs team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics.
$103,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A Clinical Research Coordinator is needed to work with Dr. Jana Jones and Dr. Struck to coordinate clinical research. The Clinical Research Study Coordinator will also cross-train on other clinical studies in the epilepsy group and serve as a back-up coordinator for these studies.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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clinical research jobs Title: research clinical manager Company: Cleveland Medical Center
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