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In this role the Research Nurse Coordinator screens, enrolls, plans, implements, and evaluates protocol-related care of participants and data for assigned research projects. Christiana Care Health System is currently seeking a Research Nurse Coordinator with two years of Oncology Clinical experience for our Cancer Research Department at the Helen F. Graham Center & Research Institute in Newark, DE.
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Research Nurse Coordinator (RN) Follows study-specific protocol guidelines, communicates, and interacts with investigators, hospital staff, department manager, sponsoring agencies, and others to effectively perform clinical research activities.
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Coordinates all aspects of protocol treatment and monitoring and ensures everything is completed and documented. Creates methods and systems to ensure patient compliance with protocol procedures, uses a problem-solving process when non-compliance occurs.
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Submit protocol, informed consents and necessary documents to Institutional Review Board (IRB) for approvals; communicate with IRB on a regular schedule if applicable. Attend IRB meetings for protocol review, as needed.
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Join Avera as a Registered Nurse (RN) Senior Clinical Research Coordinator. This position requires close collaboration with the research team to ensure safe and compliant adherence to the research protocol and ancillary study activities.
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The Senior Clinical Research Coordinator-RN is an advanced position that involves a balance of study participant contact, research study initiation, coordination, and management of study data. Licensed as a Registered Nurse in the State of South Dakota and/or meeting the requirements of Multi-state licensure required.
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Acts as a resource nurse for protocol groups and coordinates data management. The Nurse Coordinator utilizes effective communication and collaboration skills, and ensures coordination of care with physicians, nursing staff and other disciplines/departments to facilitate positive patient outcomes.
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To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP). To perform the informed consent process following GCP. To act as a liaison among the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.
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At each of our 12 multidisciplinary disease site centers, patients have a fully dedicated team that include oncologists, surgeons, navigators, and social workers, as well as a clinical research nurse at each MDC to explore avenues for potential cutting-edge treatments in the latest clinical trials.
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The Clinical Research Nurse Coordinator is responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes responsibility for nursing assessment and patient intervention, FDA, IRB and Study compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, maintenance of drug records, study report preparation, and protocol information dissemination to investigators, health care professionals, patients, and their families.
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Coordinates disbursement of and administers protocol provided drug therapy. Ensures accurate research intervention (drug, device) by communication of dose modifications and protocol requirements to the physician investigator.
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Report and compile protocol activity and data Quadrant, Inc. is an equal opportunity and affirmative action employer. Responsible for education of clinic staff regarding clinical research. Oversee patients for changes in condition, adverse events, compliance and response to study drug, Document all findings Responsible for accurate and timely data collection, documentation, entry, and reporting.
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Maintains current protocol with revisions, amendments and current IRB approved informed consent. Communicates with physician/office staff regarding scheduling protocol specific requirements.
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Independently or in collaboration with the departmental research technician, obtains, processes, and ships clinical samples from patients in accordance to protocol guidelines. Educates faculty and hospital staff by providing written and oral presentations related to protocol treatment administration and procedures.
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In addition to customary research coordination activities, the Nurse Research Coordinator, under the direction of the principal investigator, will perform study-related assessments and procedures, such as: physical examinations, transient elastography (TE), electrocardiogram (ECG) infusion therapy, phlebotomy, and administer medications as outlined in the research protocol.
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protocol job Title: coordinator nurse
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