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Provide Global Patient Safety expertise to internal and external customers (e.g., regulatory, Affiliates, FDA, COE, Discovery and Clinical Research, Business Units). OR BS degree in health-related or scientific field with 7-10 years of experience in pharmaceutical industry, directly related clinical trial experience or experience in areas relevant to drug discovery or development, e.g. epidemiology, toxicology, pharmacovigilance, regulatory affairs.
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The Clinical Trials Office seeks a Clinical Research Coordinator (CRC) to assist with clinical trial coordination for specified disease-oriented oncology research teams.
$39,686.4 - $52,603.2 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experience: Experience in the pharmaceutical industry (preferably veterinary) with understanding of veterinary clinical studies and regulatory requirements (e.g., GCP, GLP). Plan and have oversight of clinical audit activities for veterinary Good Clinical Practices (GCP) and/or pivotal Good Research Practices studies, ensuring compliance with internal and external standards.
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Our center has more than 50 clinical research projects involving bleeding disorders, sickle cell disease, thrombosis and more. What You Will Do As a Research Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.
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