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We are seeking a Clinical Research Coordinator-C who will take on a senior research role within the Traumatic Brain Injury Clinical Research Initiative in the Department of Neurology.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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An enticing opportunity awaits you at MSK. Are you an experienced contracts negotiator passionate about being part of a team dedicated to supporting the research mission of Memorial Sloan Kettering (MSK) or have a background in clinical research and looking to expand your expertise.
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The Research Associate Clinical I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board ( IRB.
$17.24 - $27.59 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A full-time Clinical Research Coordinator position is available at the Massachusetts General Hospital (MGH)/Harvard Medical school in the laboratories of Drs. Mark Eldaief and Randy Buckner for a research project involving Transcranial Magnetic Stimulation (TMS, a form of non-invasive brain stimulation.
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Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired.
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Preferences Working knowledge of pediatric hematology/oncology clinical trials Laboratory experience processing tissue samples Credentialing as a Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or other related certification.
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High School Graduate and/or technical degree and 8 years as a Clinical Research Coordinator/Clinical Research Associate. Associate degree and a minimum of 6 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR.
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The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care.
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The Clinical Research Coordinator II will have various responsibilities related to the preparation and/or review of the scientific proposal, regulatory and IRB protocols, sponsor contracts (Terms & Conditions), conduct of research, reporting, and project closeout procedures.
$58,000 - $62,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
$87,300 - $156,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A minimum of two (2) years as a Clinical Research Coordinator within the past five years OR Current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA.
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In this role, the successful candidate The Community Clinical Research Coordinator (CRC) is an active participant coordinating of all related clinical research studies, from research planning to completion of all studies, including direct involvement in case management of study participants, study coordination, and data collection for community-engaged studies.
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