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The Research Data Coordinator 2 is responsible for data management for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center (LCCC.
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Certification as a Clinical Research Coordinator. Demonstrated experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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The Clinical Research Coordinator I (CRC) works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DF/HCC Clinical Trials Office and/or Partners HealthCare Institutional Review Board (IRB.
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This unique role allows for the clinical research nursing professional to work in the community and screen/enroll patients in all cancer disease centers with UPMC Hillman Cancer Center working as a Trials Coordinator.
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The Oncology Associate Clinical Research Coordinator (aCRC) is an active participant in the coordination of oncology clinical trials from research planning and throughout the conduct of clinical trials.
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The Clinical Research Coordinator II Non-RN (CRC II Non-RN) serves the AdventHealth Research Institute (AHRI) in the Rocky Mountain Region (RMR). + Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA.
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The Clinical Research Coordinator work within the Neuro Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator.
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Clinical Research Coordinator C (CRC-C): In addition to above, the CRC-C will have limited supervision from the project manager and will need to use more independent judgment when managing their assigned clinical trials.
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Our Plano campus is looking for an experienced Clinical Research Coordinator who will play an important part in coordinating drug treatment research trials within the Hematology and Oncology teams, as well as observational studies.
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Licenses and Certifications Preferred: Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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Experience 2-5 Years' experience as a Clinical Research Associate, Clinical Research Coordinator, Clinical Research Nurse Coordinator and proven experience as an Lead Auditor.
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Description The David Geffen School of Medicine, Department of Urology is seeking to hire a Full Time Senior Study Coordinator for pharmaceutical and industry sponsored, investigator initiated, and NIH-sponsored clinical trials.
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Summary The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to maternal health and diabetes.
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