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Role Overview: The Clinical Research Coordinator oversees clinical trials, ensuring compliance with regulatory standards. Weekly | Up to 75% travel About The Clinical Research Network: We are launching a multi-specialty Clinical Trials Site Network with a primary focus on dermatology for Phase 2 – 3 studies.
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Prepares for study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement, scheduling of biopsies and scans, facilitating RECIST form completion from the investigator, AE and ConMed form completion in conjunction with a licensed professional (CRN/APP/MD) and other tasks as needed to support the administrative conduct of clinical trials.
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Under the direction of the Brown Cancer Center Clinical Trial Office leadership and in collaboration with a Research Nurse or Clinical Research Coordinator, the Clinical Research Coordinator IV assists in the coordination of daily activities related to the conduct of oncology clinical trials.
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Working Title : Clinical Research Coordinator I (Hybrid), Cancer Clinical Trials. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, communicating non-medical trial concepts and details, and participating in the informed consent process.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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The role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry-sponsored clinical trials that bring new treatment options to our patients; and complete research billing review in Epic; and facilitate research invoicing for industry-sponsored and federally-funded clinical trials; and work collaboratively with Oncology Research Coordinators and Grants Management colleagues to support accurate billing and invoicing.
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Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.
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As a Laboratory Research Assistant you will perform high-level medical laboratory processing procedures for specimens received on patients enrolled in clinical trials. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Please click here to learn more about our research offerings.
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The individual will be responsible for assisting the Department faculty in conducting National Institute of Health (NIH), industry sponsored clinical trials, and/or investigator-initiated trials.
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Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval.
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Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols.
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The OHSU Knight Cancer Institute Clinical Research Coordinator is responsible for implementation and overall management of oncology clinical trials. Research experience with some knowledge of clinical trials.
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For the scientific advancement of clinical research, CMRPD services include comprehensive clinical trials monitoring, regulatory, pharmacovigilance, protocol navigation and development, and programmatic and project management support for facilitating the conduct of 400+ Phase I, II, and III domestic and international trials on a yearly basis.
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This position provides legal expertise and support across all business functions engaged in registered clinical trials (Phases 1-4), and other evidence generation activities including investigator-initiated trials, real world evidence, translational research, health economics and outcomes research.
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clinical trials research jobs Title: clinical nurse Company: Clinical Management Consultants
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