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Clinical Research Coordinator certification (CCRC) or Research Professionals certification (ACRP or SOCRA) Two to three years of work experience in clinical research with emphasis on IRBs, Ethics Committee and Human Subjects review in pharmaceutical, biotechnology, or academic research settings.
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The Center for Cancer Cell Therapy (CCT) at Stanford University is seeking a Clinical Trials Regulatory Specialist 2 to be responsible for the administration and regulatory compliance of clinical research within the university and representing the university with external regulatory agencies, both domestic and international.
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The Clinical Trials Regulatory Specialist will work within in multidisciplinary teams of highly skilled physicians, research scientists, cell manufacturing experts, and clinical research staff to conduct innovative early phase clinical trials according to Good Clinical Practice and all relevant institutional, state, and federal policies.
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With input from PI(s), draft research protocol documents and clinical research informed consent forms. Experience with regulatory affairs in an academic research environment.
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Our client is seeking a Regulatory Affairs Manager for the Murtha Cancer Center Research Program (MCCRP), Uniformed Services University of the Health Sciences (USUHS) and John P. Murtha Cancer Center (MCC) at the Walter Reed National Military Medical Center in Bethesda, Maryland.
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Ensure compliance with regulatory requirements for working with animals in biomedical research, including the Animal Welfare Act & Regulations, the Guide for the Care and Use of Laboratory Animals, local policies, and other applicable regulations.
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The Clinical Research Coordinator is also responsible for keeping all data and source documentations, adverse event reporting, and IRB regulatory files. 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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Vanderbilt Health - Executive Search Team is conducting a national search for a Division Counsel - Compliance & Regulatory Attorney with a strong regulatory and compliance background, including expertise in federal and state fraud, waste and abuse laws and related regulations, Medicare and Medicaid (TennCare) regulations and conditions of participation, and clinical research compliance.
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The Clinical Research Resources Office (CRRO) Regulatory Education Manager will manage two important aspects of the HRPP: the Research Professionals Network (RPN) and the human/clinical research education and training for Boston University and Boston Medical Center researchers (PIs and study staff.
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UPMC Hillman Cancer Center is currently hiring a regular full-time Regulatory Specialist to help support the Medical Oncology Clinical Research Services team located within the Hillman Cancer Center in Shadyside/Pittsburgh, PA. This role will support multiple disease center working Monday through Friday daylight hours.
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The regulatory coordinator is responsible for overseeing the regulatory affairs of the UW Hematologic Malignancies Research Program's clinical trials and research studies.
$5,457 - $5,834 a monthFull-timeExpandApply NowActive JobUpdated 1 days ago - UpvoteDownvoteShare Job
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Based out of the Washington, DC area, The Travel Clinical Research Coordinator Based primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
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The Clinical Research Coordinator (CRC) is an integral and essential member of the ACC CRU Research Team. We are looking for an enthusiastic, professional and committed team member to work closely with our clinical research investigators, Research Team Leaders, our clinical research nurse(s), and regulatory coordinator.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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In collaboration with clinical trial teams across the country, will support the clinical trial research goals of the CTCC by monitoring numerous centers specified trial cycle metrics and protocol fidelity, and oversee local, institutional and federally-required regulatory compliance across the network of collaborators.
$55,200 - $96,600 a year depends on experienceFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Manages and coordinates all facets of assigned clinical protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. Collect specimens (blood, urine, CSF, tumor samples) for clinical and research testing.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated 0 days ago
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