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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Clinical Research Coordinator opening.
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Supporting PIs in the development and growth of the research cores currently consisting of biomarker, neuroimaging, clinical cognitive, and data science. a clinical research environment, statistical analyses with supervision, and coordinating data acquisition in a.
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The Data Manager III will provide data management support for new and ongoing HIV and other emerging infectious disease studies conducted by MHRP, EIDB, and affiliated programs, involving clinical observational research, laboratory research, clinical trials, and other research studies.
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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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The Division of Endocrinology is seeking a full-time Clinical Research Associate for an exciting, expanded role in cutting-edge diabetes research. The Clinical Research Associate role will be responsible for managing research-related activities for both epidemiological and novel interventional studies in diabetes (Type 1, with opportunities in Type 2), Under direction of the PI, assists in performing biomedical research.
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The Research Associate Clinical I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board ( IRB.
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We support a vibrant and diverse research enterprise , with programs in basic, translational, clinical, population, and data sciences. Faculty enjoy internal collaborations and joint appointments with many clinical departments and centers, includingCenter for Regenerative Biotherapeutics, Center for Individualized Medicine, Research Department of Artificial Intelligence and Informatics, Robert and Arlene Kogod Center of Aging, and Mayo Clinic Comprehensive Cancer Center.
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12+ years of experience in designing, conducting, and leading biomarker research leveraging wearable devices, health /medical devices, and EHR/EMR health data, and conducting clinical studies with human subjects both in lab and field settings.
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The Clinical Research Coordinator is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, performs noninvasive cardiovascular tests according to study protocols, and conducts small group coaching sessions.
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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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Under the direction of the Clinical Team Manager, the incumbent will directly supervise, mentor and train Clinical Research Coordinators, Research Nurses, and/or Data Coordinators, ensuring that all research activity adheres to applicable International, Federal, State, and Institutional laws, policies, procedures and requirements.
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Assistant Clinical Research Coordinator. Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies and may receive training and development to prepare and advance for journey-level work at the next level within the series.
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The Division of Rheumatology, Allergy and Immunology (DRAI) at Massachusetts General Hospital (MGH) is seeking an intellectually curious and highly organized individual with supervisory experience to serve as a Research Project Manager in a clinical trial which will test two different treatment strategies for gout.
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clinical research jobs Title: data review
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