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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 Community Practice Clinical Data Coordinator at Trial Library will play an integral part in expanding access to cancer clinical trials by pioneering pre-screening efforts in community oncology settings.
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The Office of Clinical Trials Activation (OCTA) provides business support to investigators and study teams initiating and conducting clinical trials. OCTA services improve compliance and enable a more rapid activation of clinical trials to increase and improve patient care and provide cutting edge treatment opportunities for our patients and advance our research mission.
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Option to do teaching, lectures, research, clinical trials. Schedule: 80% clinical, 20% teaching/academics. Disneyland, Six Flags, Universal Studios & Knotts Berry Farm. Able to incorporate Integrative Health, that have an established Integrative Medicine Dept.
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Participate in clinical trials, either institutional, pharma, or cooperative clinical trials through Roswell Park Cancer Center affiliationProgram that prioritizes social responsibility, respect, dignity, sensitivity, advocacy and community service - with a mission to improve health and life at the individual and community levels.
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Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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During the one-year fellowship, the F.A.S.T. fellow will learn about clinical trial design, including novel clinical trials for rare genetic pediatric NDDs including N-of-1 trials, development of specialized programs for clinical management of these conditions with accommodation of experimental treatments, and new outcome measure and biomarker development for these populations.
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Rheumatology Services include acute and chronic rheumatic diseases, diagnostic and therapeutic intra-articular and soft tissue injections and aspirations, bone density and clinical trials.
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Then you might be a great fit for a Senior Clinical Research Coordinator role with DaVita Clinical Research (DCR)We are looking for a highly motivated, positive and innovative senior level Clinical Research Study Coordinator (Research Coordinator) to lead in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices.
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In addition to adopting MSK standards of care, we collaborate on clinical trials and research in a variety of health services research areas such as geriatric oncology, palliative care and medical informatics.
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Clinical Highlights: We are a COC accredited cancer program Established fellowship program with 2 Hematology/Oncology fellows SLUHN Cancer Center received the National Cancer Institute’s National Clinical Trials High Performance Site Award (2017, 2018.
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The Clinical Research division, has successfully conducted major ground breaking innovative trials partnering with Harvard Clinical Research Institute, Duke Clinical Research Institute, and many Pharmaceutical and Biotechnology companies.
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This role plays a pivotal role in coordinating and overseeing clinical operations of all assigned Clinical Research Nurse and Clinical Trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies.
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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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Join us as we further our reputation as a leader in clinical care, healthcare research, education and social commitment. The Clinical Supervisor manages research project activities ensuring the quality and integrity of data collection, and trains, manages, and supports student staff and interns, reviewing work products to ensure study protocol is followed as written and approved by the institution’s IRB. This position will assist with the supervision of research coordinators.
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clinical trials jobs Title: social Company: Cincinnati Hospital Medical Center
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