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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. 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 Veterinarian will also participate in research support of GLP and non-GLP studies involving both USDcovered and non-covered species; this individual may manage clinical aspects of the studies, provide guidance on animal model and protocol development, and participate on the IACUC through conducting veterinary reviews.
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The Clinical Research Associate position at Medpace offers. Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement.
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Applicants should demonstrate a strong interest in multidisciplinary clinical, educational, and research collaboration and excellent interpersonal communication and leadership abilities.
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Dr. Han's research lab is in acute need of a Clinical Research Coordinator (CRC) to assist with the currently ongoing study Glaucoma Drainage Device and Endothelial Cell Density Loss Compare (DECLARE) trial, the Clarifying the Optimal Application of SLT Therapy Trial (COAST) trial and other clinical studies.
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High School Graduate and/or technical degree and 6 years as a Clinical Research Coordinator/Clinical Research Associate. Bachelor’s degree and minimum of 2 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR.
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The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI), and/or the Associate Director for the Clinical Research Programs.
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The Division of General Internal Medicine (DGIM) at Massachusetts General Hospital is seeking a Research Assistant (Clinical Research Coordinator) to join our research team.
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Years’ experience: Minimum of two (2) years’ experience coordinating research protocols OR (2) years' experience in cancer research OR certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), or 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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The Division of Endocrinology is seeking a full-time Clinical Research Associate for an exciting, expanded role in cutting-edge diabetes research. The Clinical Research Associate role will be responsible for managing research-related activities for both epidemiological and novel interventional studies in diabetes (Type 1, with opportunities in Type 2), Under direction of the PI, assists in performing biomedical research.
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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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Works closely with AHRI Core managers to schedule clinical operations to facilitate the initiation and completion of clinical research studies, the CRC II also promotes Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Lead and Director of deviations in conduct, patient status, issues relevant to the integrity of the trial and/or the safety of research subjects.
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Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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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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Represents the department and investigators at local, regional and national meetings; facilitate effective communication among staff, PIs and other research/clinical professionals, senior leaders of UAMS, and study sponsors.
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clinical research jobs Title: senior clinical trial associate
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