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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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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.
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The Clinical Research Coordinator 2 is responsible for identifying eligible patients for research and ensuring that research protocols are carried out accurately. St. Luke’s Health System in Boise is seeking a Clinl Research Coordinator 2 to join our team.
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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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The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
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Hiring Manager is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Study Coordinator, Clinical Research Coordinator, Clinical Research Regulatory.
$30 - $35 an hourExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Senior Clinical Research Assistant is a highly organized and motivated clinical research coordinator who assists principal investigators with outpatient clinical trials related to type 1 and type 2 diabetes.
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To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Trial Safety Associate for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.
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Serves as a supporting clinical research coordinator to CRC/CRN II and Sr. CRC/CRN for highly complex protocols. The Cardiovascular Data Science (CarDS) Lab at Yale University is currently seeking a Clinical Research Coordinator to join our team.
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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.
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A minimum of 2 years of on-site monitoring experience is required, however monitoring experience may be waived if relevant Novo Nordisk experience is demonstrated in GCP-related clinical research.
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Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role. The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values.
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Manages mutually beneficial relationships with external partners relevant to the planning and implementation of clinical trials and improvement/innovation projects for NACD and Novo Nordisk (e.g., clinical trial site staff, clinical research vendors.
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Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) Certified Research Associate (CRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or comparable.
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Working with Clinical Research team and key personnel including the Executive VP of Clinical Research, this highly skilled and team-oriented Medical Director will be a physician and will have subspecialty training in Nephrology or Infectious Disease or Rheumatology and have at least 1.5 years of clinical research and development experience.
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clinical research jobs Title: research clinical project manager Company: Cleveland Medical Center
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