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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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Thoroughly reviews complex study protocols, Informed Consent Documents (ICD), draft sponsor Clinical Trial Agreements (CTA), and budgets to identify all the Emory Healthcare (EHC) and/or Grady billable items and services required of the study which might generate a CPT code.
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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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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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Join two established neuro-oncology faculty in a comprehensive program that includes neurosurgery, radiation oncology, neuro-pathology, neuro-radiology, rehabilitation services, clinical trials staff (both late-phase and Phase 1 programs), a dedicated support staff, and many other components - all at a thriving, growing NCI-designated cancer center.
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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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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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Multidisciplinary programs in Neuromuscular Medicine (EMG/NCV lab), Tuberous Sclerosis Complex Clinic, Ketogenic Diet Clinic, Neurofibromatosis Clinic, CMT Center of Excellence, PPMD-certified muscular dystrophy clinic and a close tie to the MDA.High quality academic and clinical program with ongoing clinical trials.
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The person will support Infectious Disease Physician Investigators in clinical research ranging from observational trials to investigational drug/product trials, including investigator-initiated, government funded, and industry-sponsored trials.
$42,953 - $77,315 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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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We are a diverse team of experienced physicians and clinical scientists who collaborate to delineate early phase clinical development strategies, design innovative phase I-IIb clinical trials, develop and validate novel surrogate endpoints, and translate scientific ideas to proof of concept studies in targeted patient populations.
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Early phase clinical/translational research expertise, including experience in designing, monitoring, performing and interpreting early phase clinical trials and solid knowledge of biomarkers, surrogate endpoints, biostatistics, and safety reporting.
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The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the program.
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Performs gating, analyses and scientific review of high dimensional flow cytometry data collected from immuno-oncology clinical trials. Follows Navigate Flow Cytometry Subject Matter Expert (SME) guidance and training to deliver on fit-for-purpose analytical strategies that fulfill mechanistic endpoints of investigational clinical studies.
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The Department of Neurology is seeking a Statistical Programmer Analyst who will support the BIOS Clinical Trials Coordinating Center's (CTCC) Research Program and Clinical Trials Unit, which manages multi-center, 20+ million dollar federally funded clinical trials and multiple site-specific pharmaceutical sponsored trials.
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complex clinical trials outdoor jobs Company: Emory University
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