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The role involves conducting ad hoc analysis, developing and managing dashboards, and monitoring KPIs. This role requires proficiency in SQL, statistical analysis, data visualization, and collaboration.
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We seek an organized, highly motivated, full-time Clinical Research Coordinator I (CRC) to join our Dystonia Partners Research Bank team in the Department of Neurology at Massachusetts General Hospital.
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Our core team includes 4 Neurologists, with our PI, Nutan Sharma, M.D., Ph. D., 2 Research Coordinators, a Clinical Research Fellow, a Staff Assistant, and a Clinical Research Program Manager/Genetic Counselor.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
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Clinical Research Coordinator, Norwalk, CT. Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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The Travel Clinical Research Coordinator will be mentored by their CRC Lead, Site Manager, Senior Manager, and other leaders within clinical operations. Based out of New York, NY area, The Travel Clinical Research Coordinator 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 predominately functions as the key coordinating lead for the local University of Chicago SuperAging site activities related to data collection and participant visits.
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JOB SUMMARY: The Clinical Research Nursing Coordinator works collaboratively with the Principal Investigator and other research staff to support study implementation. Clinical Research Nursing Coordinator.
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The Clinical Research Coordinator (CRC) will perform independently or with general direction to execute, manage, and coordinate upwards of 10 research projects, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
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Based out of the Chicago, IL area, the Travel Clinical Research Coordinator 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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Our mission to help LGBTQ people lead healthier, happier lives is supported by our comprehensive array of client-centered services including primary care, mental health, psychiatry, sexual health, pharmacy, case management, nutrition, clinical research, housing services and a food pantry.
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Today, our team continues to expand across the globe, with over 350 employees across the US, Europe, Australia, and Asia. The Role:Ora's Clinical Research Coordinator I (CRC) has close relationships with the subjects who participate in our clinical trials located regionally, domestically, and at times, internationally.
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Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Clinical Research Coordinator Assistant 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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As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases.
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PREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Full-time Clinical Research Coordinator, Poughkeepsie, NY.
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Title: clinical research coordinator Company: M3 Usa
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