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Job Description & Requirements Clinical Trials Oncologist StartDate: ASAP The LSU Health New Orleans/LCMC Health Cancer Center in historic, highly desirable New Orleans seeks a Medical Oncologist.
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The role represents the CPQP function on drug development teams, leads CPQP sub-teams, and owns strategy and delivery on posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory and CMC groups.
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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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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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Oversee all EDC,and IRT vendor contracts for assigned clinical trials. Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events.
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The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials. The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.
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QUALIFICATIONS Education: Requires MD or MD/PhD, Immunology, Inflammation and Neurology specialty required, but other specialists with experience in GI, Rheumatology, Allergy and Hematology clinical trials will be considered.
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Position Summary Reporting directly to the Executive Director of the Clinical Trials Office (CTO), the Associate Director for Operations (Associate Director) is responsible for the management and oversight of business operations and finance in the CTO at the Vagelos College of Physicians and Surgeons (VP&S) and NewYork-Presbyterian Hospital (NYPH.
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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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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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Experience drafting and negotiating clinical trial agreements. Experience with clinical trial and/or research agreements with ability to handle increasing levels of responsibility. Support strategic initiatives of the VP/ Deputy General Counsel and EVP/ General Counsel.
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Provides subject expertise on a diverse portfolio of development programs and different therapeutic modalities including small molecules, biologics and cell gene therapy for Gilead’s global 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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ADDITIONAL JOB RESPONSIBILITIES:The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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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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clinical trials jobs Title: clinical director Company: Biospace in Chalmette, Louisiana
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