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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 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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This position will involve internal CAP/CLIA lab support, assay development responsibilities and clinical trials support. The candidate should have a strong interest in providing pathology support for biomarker development programs across oncology and hematology as well as an interest in clinical trials support/enablement.
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Under general supervision, the Trauma/Burn Clinical Research Assistant works with UCSD faculty and principal investigators in the management of study participants enrolled in clinical trials related to the study of trauma, burn, and wound treatments.
$34.78 - $55.92 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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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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We also have a strong relationship with pediatric movement disorders neurologists at CHOC. For clinical trials activities, the CIRM-funded UCI Alpha Stem Cell Clinic and the Center for Clinical Research provide robust infrastructure for clinical trials, and we are a Parkinson Study Group clinical trials site.
$220,000 - $289,940 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts.
$138,904 - $165,489 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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AAMC’s Research Instititue with active participation in cancer clinical trials, including industry-sponsored and cooperative group trials, and the Johns Hopkins Cancer Research Network [JHCRN.
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These activities may occur at various stages of the clinical trials, including study start-up, maintenance, close-out, and/or archival. Prior experience working with or managing Trial Master Files for global clinical trials preferred.
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The UW Clinical Trials Institute Contract Manager reports to the SMPH Director of Contracts within the Fiscal Affairs Division, and will participate regularly in the Clinical Trials Strategic Leadership Team meetings and other CTI-specific activities.
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Clinical Operations Oncology is responsible for the worldwide execution of all Phase 1 through 3 clinical trials within the Oncology Therapeutic Area. Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead's products.
$154,020 - $199,320 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with clinical trials regulatory affairs, or related clinical trials experience such clinical research coordinator experience. Review, provide feedback, and approve Medicare coverage analysis and budgets for complex clinical trials; serve as point person from study team for budget negotiations.
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CRD also provides operational support for clinical research and supports clinical trials management, regulation, pharmacovigilance, and protocol development/protocol navigations. Prior experience in clinical trials and/or experience in data management and collection.
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clinical trials jobs Title: clinical director marketing in Chalmette, Louisiana
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