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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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With 15+ years of experience in this space, our teams have supported 1000s of clinical trials, 100s of EDC builds for a multitude of Sponsors/CROs. With a long-standing alliance with Medidata (now Dassault Systems), the leading EDC platform solution provider, we have been successfully implementing Medidata’s best-of-the-breed products to help execute very complex mega-trials for our premium customers.
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NCI Community Oncology Research Program grant (NCORP) recipient with access to current, relevant clinical trials. Caring and attentive team of support services including genetic counselor, nutrition support, social work, nurse navigation, behavior therapist and lymphedema specialists.
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The Clinical Research Coordinator II works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DF/HCC Clinical Trials Office and/or Partners HealthCare Institutional Review Board (IRB.
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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 Postdoctoral Research Fellow will contribute to ongoing maternal and child health clinical trials conducted by the research group including an NIH-funded clinical trial of zinc for young Tanzanian infants with sepsis and two clinical trials funded by the Bill & Melinda Gates Foundation that are being conducted in Tanzania focused on feeding options for preterm infants and iron dosages in multiple micronutrient supplements for pregnant women.
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Successfully manage CROs and establish relationships to develop biomarker assays, monitor assay qualification/validation at CROs, as well as bioanalytical/biomarker testing in the clinical trials.
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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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A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers.
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Participate in an individualized training/orientation program geared to teaching or reinforcing the principles of Clinical Trials Nursing practiced at MSKCC. Clinical Trials Nurse - Bone Marrow Transplant Outpatient setting.
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Ph. D. or DrPH degree with experience in cancer clinical trials design and implementation of statistical activities during trial conduct. Ph. D. or DrPH plus experience in cancer clinical trials design and implementation of statistical activities during trial conduct.
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The Regulatory Coordinator I will act as a resource to investigators and staff for interpretation and execution of complex clinical research regulations, policies & procedures concerning the conduct of clinical trials, including those of the FDA, HHS, UCSD IRB, and the CTO. This position requires regular interaction with a variety of internal and external contacts including Cancer Center investigators and staff, UCSD IRB staff, study sponsors and/or their representatives.
$31.04 - $55.92 an hourExpandUpdated 7 days ago - UpvoteDownvoteShare Job
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In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States.
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The Clinical Research Monitor works in partnership with the AFT Project Manager and individual study teams to complete all site monitoring activities across assigned AFT projects and ensures all participating sites are compliant with Good Clinical Practice (GCP), SOPs, policies, and regulatory requirements throughout the life of assigned clinical trials.
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The Clinical Research Monitor will work under the Executive Director of Clinical Trial Operations and the Associate Director of Clinical Trial Operations to oversee activity at Alliance for Clinical Trials in Oncology sites participating in Alliance Foundation Trials (AFT) clinical trials.
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