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Individual is responsible for histocompatibility laboratory compliance with regulatory and accreditation agency standards, quality assurance, development of laboratory processes clinical protocols and budget preparation monitoring.
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Job DescriptionThe Clinical Research Coordinator B/C will assist in oversight, execution, and regulatory compliance of human subject research for clinical research projects exploring investigational treatments and diagnostic tools relating to the care of patients with Epilepsy.
$42,953 - $77,315 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Research Coordinator I assists with all data and source documentation, adverse event reporting and maintenance of complete regulatory files, also as a part of the learning experience.
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2+ years' experience in research compliance or research administration in an academic or clinical setting. The ORSC educates and supports the University research community with regulatory guidance concerning human subjects research (Institutional Review Board), animal research (Institutional Animal Care and Use Committee), use of biohazardous agents and use of recombinant or synthetic nucleic acids (Institutional Biosafety Committee), and financial conflict of interest in research (FCOI.
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Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing.
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At Baylor Scott & White – McLane Children’s Hospital in Temple, we are committed to providing our CRNAs with a comprehensive and competitive benefits package to support their well-being and professional growth.
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The department currently supports four full-time medical physics faculty, six clinical physicists, four dosimetrists, two medical physics assistants, a dedicated linear accelerator engineer, and information systems and research staff, inclusive of research scientists, post-doctoral fellows, and clinical research associates.
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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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The position will work closely with the Director, AD of Clinical Operations, investigators, and study team members (e.g. clinical research nurses, specimen technicians, statisticians, regulatory specialists, and financial analysts), as well as clinical and hospital staff to manage the day-to-day operations and objectives in support of the trial portfolio.
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F) Under the direction of the of the Director, Healthcare Analytics, is responsible for CORE data security in compliance with Yale New Haven Hospital /Health System, Yale University and funding agency policies.
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Collaborate with Research & Development, Scientific Affairs, and Laboratory staff in any way applicable to support Clinical Trials. Ensure all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP), Medicines and Healthcare Products Regulatory Agency (MHRA), Food and Drug Administration (FDA), International Organization for Standardization (ISO), etc.
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Regulatory Coordinator Oncology Clinical Research Unit [CRU] GENITOURINARY Clinical Research Program [GU] Position Description, Occupational Summary Perform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] Genitourinary Clinical Research Program [TNA.
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BJCs patients have access to the latest advances in medical science and technology through a formal affiliation between Barnes-Jewish Hospital and St. Louis Childrens Hospital with the renowned Washington University School of Medicine, which consistently ranks among the top medical schools in the country.
$15 - $999.99 an hour depends on experiencePart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintain compliance with clinical genetic testing regulatory agencies and proficiency programs (CAP, CLIA, NYS Department of Health). 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.
$50.11 - $80.21 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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HemaCare’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.
$39.86 - $49.23 an hourExpandApply NowActive JobUpdated 9 days ago
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