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Job Summary: The Clinical Laboratory Scientist is responsible for performing moderately complex and complex laboratory tests, as defined by CLIA, in hematology, chemistry, urinalysis, microbiology, blood bank and serology.
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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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Competencies: - Clinical experience, understanding of, and comfort working with patients of all ages who suffer complex medical and psychiatric problems; ability to work with the families of such patients, and ability to help patients and families understand and access the resources required to support care.
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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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Description Clinical Research Coordinator B ResponsibilitiesThis individual will work under general supervisionThe CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training.
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As a New Grad RN, you will participate in a year-long residency program, customized to fit you, your needs and your pace, where you will provide direct nursing care, be paired with a coach that guides you toward success, develop clinical judgement, cultivate excellent communication skills and acquire complex nursing skills.
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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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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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This one-year fellowship opportunity is for physicians to be mentored in the translational neuroscience program headed by Elizabeth Berry-Kravis, MD, PhD. As the leading investigator in multiple NIH-funded research programs and industry-and foundation-sponsored clinical trials, Dr. Berry-Kravis has established Rush University Medical Center as an international destination for rare disease treatment and research in the area of pediatric neurodevelopmental and neurogenetic conditions.
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The Neuro ICU at Barnes-Jewish Hospital is a specialized, state-of-the-art unit dedicated to the care of patients with complex neurological conditions. The BJC RN Career Ladder differentiates BJC as the place for nurses to work in the greater St. Louis area.
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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. Always needs to have positive attitude, robust attention to detail, strong work ethic and ability to maintain confidentiality.
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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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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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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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Provide support to Clinical Trial Management teams by processing documents in the electronic Trial Master File (eTMF) according to Xencor Standard Operating Procedures (SOPs), Work Instructions (WIs), and trial-specific processes such as the TMF Plan and TMF Index.
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complex clinical trials shift work jobs Company: Emory University
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