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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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ResponsibilitiesA day in the life of a Clinical Research Nurse at Hackensack Meridian Health may include:Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
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Our ideal candidate would be an early to mid-career medical oncologist focused on thoracic malignancies with leadership skills to help drive the growth and visibility of our multidisciplinary program here at Mayo Clinic AZ. The successful candidate will be able to partner with our internationally recognized surgical, medical, and radiation teams in a multidisciplinary clinic; initiate, run and develop clinical trials; recruit future colleagues and drive innovation across the spectrum of care.
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Assist with completion of initial IRB submissions, annual continuing reviews, amendments, and reliance agreements for clinical trials• Prepare FDA submissions (1572, IND, IDE, HUD etc.) Ensure patient safety is a top priority in conducting clinical trials.
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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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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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Analyze unstructured and/or structured biological data from biosensor clinical trials and evaluate biosensors performance to support product designs. This Sr. Engineer role supports our next-generation biosensor product design and development, focusing on clinical data analyses and sensor algorithm verification and improvement.
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Additionally co-resident with CMRR is the Center For Clinical Imaging Research where clinical research and trials utilizing MRI, MRS, PET/CT, and CT can be performed in a controlled and less hectic environment.
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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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The center will function as a hub for microbiome data partnerships and a conduit for microbiome-based clinical trials. The CHOP Center for Microbial medicine will focus on developing microbiome-informed clinical diagnostics and microbiome-based therapeutics.
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The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
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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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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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PRINCIPAL DUTIES AND RESPONSIBILITIES: Study Start-Up·Oversight of the clinical trials start-up process from receipt of proposal materials, protocol development, IRB submissions, through site(s) activation.
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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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clinical trials jobs Title: social worker Company: Cincinnati Children's Hospital Medical Center
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