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The Clinical Research Nurse I serves as Clinical Research Nurse 1 for phase I, II and III oncology clinical trials conducted in the Lombardi Clinical Trials Office (Lombardi CTO) at Lombardi Comprehensive Cancer Center.
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The Clinical Research Nurse II works for the Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University.
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Under the Director of Clinical Trials and the direct supervision of the Clinical Research Nurse Manager, coordinates and manages clinical trials in accordance with federal and state regulations, Institutional Review Board (IRB) approvals and Connecticut Children's policies and procedures.
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As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical trials, ensuring adherence to protocol requirements, and providing compassionate patient care throughout the research process.
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Coordinate patient care activities and participate in the conduct of studies for patients enrolled in clinical trials for multiple services including medicine and radiation oncology, etc.
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Meets requirements of Clinical Trials Chemotherapy Nurse 50% Abides by requirements in accordance with the Oncology Nursing Society's Manual for Clinical Trials Nursing.
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One year of clinical nursing experience One year of clinical research experience is preferred One year of experience treating oncology patients is preferred About Sarah Cannon Research Institute Sarah Cannon Research Institute (SCRI) is one of the world's leading oncology research organizations conducting community-based clinical trials.
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Accountabilities (For Non-exempt Employees Include Percent of Effort): Meets requirements of Clinical Trials Chemotherapy Nurse 50% 1. Follow policies and procedures for clinical trials.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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The oncology clinical research nurse works independently under the general supervision of the Clinical Trials Office Management and Leadership and the Principle Investigator for the specific protocol in order to proficiently support the safe, high quality and compliant conduct of oncology clinical research and ensure the protection of the patient.
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Reviews the Beacon Build Template in collaboration with the Physician Investigator for all trial patients enrolled onto clinical trials within the assigned or covering DMG. Ensures treatment plan is correctly built into Beacon Build Template and communicates promptly with the Investigational Pharmacy team to ensure timely completion.
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The role of the Clinical Research Nurse I is introductory, with assignments provided at a task level, and focused on less complex clinical research trials and processes. The Clinical Research Nurse I performs a variety of clinical and non-clinical tasks associated with conducting clinical research, and within the scope of licensure.
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Purpose: UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse I (RN) to help support the Clinical Research Services team located at the Hillman Cancer Center in Shadyside/Pittsburgh, PA & at the UPMC Magee Women's Oncology Research program in Oakland/Pittsburgh, PA. This role will support various Oncology Disease Center program studies working Monday through Friday daylight hours.
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University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research RN (Open Rank) Position #: 748446 - Requisition #: 34387 Job Summary: The Cancer Clinical Trials Office (CCTO) at the University of Colorado Cancer Center is seeking to employ a full time Clinical Research Nurse (RN.
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As a Clinical Research Nurse I at ICON, you will play a pivotal role in conducting clinical trials, ensuring patient safety and protocol adherence, and contributing to the advancement of innovative treatments and therapies through expert clinical care and research management.
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