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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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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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Basic biostatistics and ability to interpret data from clinical trials and outcomes research. Clinical epidemiology and population health management. Our programs were developed in collaboration with Stanford Medicine and is based on 20+ years of research on over 70,000 patients across six randomized clinical trials.
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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 Clinical Research Coordinator will work with the principal investigator to oversee clinical trials including patient recruitment & scheduling, data collection & management, and ensuring compliance with IRB regulations.
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Ability to participate in Graduate Medical Education and clinical research trials. A strong referral base including Interventional Pain Management, Primary Care, Neurology, Neurosurgery, and Rheumatology among others.
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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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In collaboration with the Associate Dean for Cancer Clinical Research and the Administrative Director of the Cancer Institute Clinical Trials Office, the Workforce Development Educator and Trainer supports the growth and development of the Penn State Clinical Trials Office (CTO) by achieving strategic objectives including overseeing multiple project activities related to training and education of clinical research staff and investigators.
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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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Familiarity with data management and visualization tools and collaborating with computational biology to analyze complex data sets emerging from clinical trials. Knowledge of clinical trial methodology, regulatory requirements governing clinical trials, companion diagnostics/in vitro diagnostics, protocol design, and/or experience in development strategy preferred.
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The Manager, Biomarker Operations will work closely with cross-functional teams, including Clinical Operations, Data Management, and Translational Scientist, to ensure successful delivery of biomarker data to support clinical trials.
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Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
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Regulatory Coordinator Oncology Clinical Research Unit [CRU] Brain TUMOR CLINICAL Research Program [BTC] Position Description, Occupational Summary Perform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] TEAM Clinical Research Program [BTC.
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DCR is based in Minneapolis, MN and operates in locations across the US.We are dedicated to improving the lives of our kidney care patients through:· Industry sponsored clinical trials in End Stage Kidney Disease and Chronic Kidney Disease· Internal prospective and retrospective research that helps inform the clinical care of ourdialysis facilities and answer critical questions.
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The ideal candidate is a mid-career clinician with extensive experience managing HIV and Sexually Transmitted Infection (STI) Treatment and Prevention and an interest/experience in program management, grant writing, clinical trials, and teaching.
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clinical trials management jobs Title: operations Company: Boston Pharmaceuticals
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