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Required Master’s degree in health-related field or desired Qualifications: PhD or Clinical doctoral degree (MD, PharmD) with a master’s degree in health economics, health services research, statistics, economics, or epidemiology.
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Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country.
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Expertise in the following areas: microbiology, parasitology, clinical research, epidemiology Substantial postgraduate training or certification in relevant areas. The incumbent is responsible for managing NIAID-supported clinical research, especially clinical trials, to support the development of diagnostics, vaccines, and therapeutics targeting malaria, neglected tropical diseases, and other parasitic diseases.
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Clinical Research Nurse - PRN/part time/night shift - US, Salt Lake City, UT Office-based ICON plc is a world-leading healthcare intelligence and clinical research organization.
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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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The Clinical Research Coordinator (CRC) will oversee the execution of research studies according to established study protocols. Clinical Research Coordinator - Position Overview.
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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 candidate will also benefit from GIMs active local and national collaborative clinical research partnerships [e.g. Centers for Medicare and Medicaid Services Innovation Programs (Comprehensive Primary Care Plus and Million Hearts Model) and the Pragmatic Clinical Trials Network partnership with the OSU Center for Clinical and Translational Science.
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This new joint venture will establish a fully integrated oncology research organization aimed at expanding clinical research, accelerating drug development and increasing availability and access to clinical trials for community oncology providers and patients, including those in underserved communities.
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Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care.
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The Clinical Research Coordinator (CRC) II will coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects. The Clinical Research Coordinator (CRC) II will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and coordinate operational efforts.
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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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Previous experience as an oncology research RN or clinical research in a related field. The Oncology Research Nursing Professional (ORNP) –is a Registered Nurse (RN) who works collaboratively with Clinical Research Staff including, but not limited to Physicians, Clinical Research Associates (CRA), APPs, Clinical Nurses, Pharmacists, and clinic staff to coordinate care for an assigned population of patients who are enrolled into cancer center clinical research trials.
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Works with the Animal Care and Use Program (ACUP) Clinical Research Administrator and Attending Veterinarian, protocol support staff, and investigators in preparing protocols for submission to the Institutional Animal Care and Use Committee (IACUC) process.
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Certified Clinical Research Coordinator (CCRC) preferred, but required within 2.5 years of employment. Coordinates clinical research studies of investigational medications, including but not limited to: regulatory compliance, study start-up phase, implementation of study, follow-up of research subjects, closeout of study, and study record maintenance.
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clinical research jobs Title: neurosurgeon Company: Hartford Healthcare
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