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The Clinical Research Coordinator III works under limited supervision and runs portions of clinical trials, assists with orientation and training, obtains signature for informed consent, central lab management, data management, completes expectancy reports, monitors visit preparation, submits low institutional risk trials and tracks TJU IRB submission and approvals.
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The clinical research coordinator (CRC) will be trained to conduct human neuroimaging research with a number of tools, including administration of TMS inside and outside of an MRI scanner.
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The CNB team is seeking a highly motivated and detail-oriented Clinical Research Coordinator A or B (CRC A/B) to support researchers and investigators globally using the tool. Clinical Research Coordinator A/B (Department of Neuropsychiatry.
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The Clinical Research Coordinator will assist with a range of tasks related to the research projects described above, including:The CRC will assist with the screening, recruitment, and enrollment of eligible participants for research studies, during health care encounters or by phone.
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Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). ¿ High School with 6 years clinical research experience with a CRC certification from SoCRA or ACRP.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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Required: Must have experience as a Clinical Research Coordinator, -2 years+ of Chart review experience on EMR -2+ years of EDC data entry. Data entry, Chart Review, Clinical Research Coordinator.
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CCRC - Cert Clin Research Coordinator (Preferred) Coordinates and facilitates the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated.
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Description The Center for Weight and Eating Disorders at the University of Pennsylvania Perelman School of Medicine seeks a Clinical Research Coordinator A. The candidate will help coordinate an NIH funded clinical trial.
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Proclinical is seeking a dedicated and organized Clinical Research Coordinator. Clinical Research Coordinator - Philadelphia, PA - Permanent. The Clinical Research Coordinator Will.
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Proclinical is seeking a dedicated and enthusiastic Clinical Research Coordinator who is passionate about clinical-translational research in the field of head and neck cancer.
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We are currently hiring for a Clinical Research Coordinator to work in our corporate Center City, Philadelphia office (19107). · Minimum 2 years working in clinical research preferred.
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Overall, the Clinical Research Coordinator is the site's primary liaison among research participants, the local investigator(s) and study sponsors. We have an opportunity for a Clinical Research Coordinator to join our Research team.
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This includes, but is not limited to, activities to advance health equity and disparities-focused study designs, community-academic partnerships and stakeholder engagement, inclusion and representativeness in CHOP clinical trials, interpretation and dissemination of findings in non-academic settings, and equitable translation (e.g., health services and policy research) of novel discoveries to advance patient care.
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The Oncology Research Coordinator at the client will be a crucial addition to our strong clinical program. The Research Coordinator coordinates assigned research studies both clinical and non-clinical throughout the regulatory process from initial Institutional Review Board application until protocol closure and maintains the research database.
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Title: clinical research coordinator in Philadelphia, Greenwood, Arkansas
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