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Maintain professional relationships with sponsors, Clinical Research Organizations, research teams, pharmacies, laboratories, IRB’s, and hospitals for the coordination of research activities Acquire continuing education pertinent to research and their licensed profession Ensures compliance with and knowledge of the company’s Code of Conduct by all subordinates to ensure an ethical work environment.
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Then you might be a great fit for a Clinical Research Coordinator role with DaVita Clinical Research (DCR) We are looking for a highly motivated, positive and innovative Clinical Research Study Coordinator (Research Coordinator) to lead in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices.
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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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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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Experience in coordinating clinical research studies, as a research assistant, assistant clinical research coordinator, or clinical research associate.
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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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This role provides direction in coordinating the collection and processing of research and clinical specimens (e.g., pharmacokinetics, pharmacogenomics and pharmacodynamics-related samples) for patients involved in clinical research studies in the Center for Translational Pharmacology of the St. Jude Comprehensive Cancer Center.
$65,520 - $114,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The McLean Behavioral Psychopharmacology Research Laboratory is seeking a full-time Clinical Research Assistant II (CRII) to work on several research studies involving substance abuse and drug development using magnetic resonance imaging (MRI), electroencephalographic (EEG) and other laboratory/outpatient procedures.
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While we welcome any well-qualified board-certified or board-eligible clinical neuropsychologist, we are particularly interested in those with clinical and/or research experience or expertise in geriatric neuropsychology and neurodegenerative disorders, we welcome applicants who can help contribute to our initiatives in teleneuropsychology and/or remote cognitive assessment, applications of novel digital technologies, and other modern methods of measurement in neuropsychology.
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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.
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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 related to maternal health and diabetes.
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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.
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This includes frozen sections, special stains, immunohistochemistry and electron microscopy for both clinical and research neuromuscular samples. Responsibilities Performs research and clinical diagnostic histology and electron microscopy experiments independently or semi-independently in accordance with protocols approved by the principal investigator.
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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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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
$10,000 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical research jobs Title: compliance Company: Pfizer
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