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Leads and/or assists the development of research/clinical investigations/studies projects and carries out all necessary responsibilities related to these projects. Summary: The Research Scientist will assist in developing and leading clinical research studies focused on traumatic brain injury (TBI), formulating experimental hypotheses, designing study protocols, analyzing data, preparing reports for publication, and collaborating with multidisciplinary teams on TBI-related initiatives.
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Certified as a Clinical Research Coordinator (CCRC), Clinical Research Associate (CCRA), and/or Clinical Research Professional (CCRP) preferred. Reviews research personnel training for assigned portfolio to ensure that participating personnel have received appropriate training in human subjects' research protection, HIPAA, animal research protection, Good Clinical Practices, conflicts of interest in research, responsible conduct in research, and shipping dangerous goods have been completed.
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Serve as regulatory support for Clinical Decision Support Tool (CDST) development and In Vitro Diagnostic (IVD) FDregulated clinical trials. Assists with the review of protocols, grants, contracts, clinical trials, and other research activities to ensure compliance with relevant federal and local regulations and policies of research involving human subjects, laboratory animals, select agents, utilization of recombinant DNA, and HIPAA.
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Focus areas of Subject Matter Expertise of Candidate - bio-defense, bio-intelligence, bio-threats, synthetic biology, analytical instrumentation, molecular biology, fieldwork, sample collection, bio-informatics, and/or machine learning/artificial intelligence as relevant to the research and development topics associated with bio-security and bio-intelligence.
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Project management of other research associates in support of the larger drug development project. Perform rapid, comprehensive characterization of candidate drug products to determine the physicochemical properties of the drug product and evaluate them for further drug development programs including ELISA, SRID, AUC, CD, Fluorescence spectroscopy, DSC, ITC, UV/Vis spectroscopy, FTIR, SLS and HPLC.
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Serve as a resource to lead development team members for assay requirements, and logistics to conduct drug development activities for small molecule compounds from the preclinical stage through to the initial clinical stage.
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The NIMH mission is to transform the understanding and treatment of mental illnesses through basic and clinical research, paving the way for prevention, recovery, and cure. Experience working with biomedical data repositories and/or biobanks (e.g. The Adolescent Brain and Cognitive Development Project (ABCD), OpenNeuro, UK Biobank, GTEX.
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A national certification as a Medical Technologist (MT), Clinical Laboratory Scientist (CLS), Medical Laboratory Scientist (MLS) or through the American Society for Clinical Pathology (ASCP) is a plus.
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Minimum of 1 year experience in research, pharmaceutical and/or vaccine development field. Research & Development. Perform reagent preparation, routine cell culture and participate in new assay development and preclinical testing utilizing aseptic techniques.
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You will have oncology clinical drug development experience, demonstrated leadership, and be able to critically evaluate the science, clinical data and competitive landscape that underlies these programs.
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DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation.
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Supervise intern documentation, including maintenance of charts in a complete, timely and legible form, including parent information forms, consent forms, data collection forms, progress notes, and treatment plans and goals as required by state DHMH Qualifications include:•LCSW-C, LCPC, or LMSW, LGPC required; OR Requires a Psy. D. or Ph. D. in Psychology with a specialty in clinical/ developmental psychology•Excellent customer service and public relations skills required.
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Protein purification from milligram to gram scale and performance of routine analytical characterization to support research projects for drug discovery. The Research Associate II/Associate Scientist I is responsible for purifying and characterizing proteins in support of the Biologics discovery research pipeline.
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The National Center for Advancing Translational Sciences (NCATS), a major research component of the National Institutes of Health (NIH) and the U.S. Department of Health and Human Services, is seeking applications from exceptional scientists to serve as the Director of the Early Translation Branch (ETB), Division of Pre-Clinical Innovation (DPI.
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Lead and shape future clinical development strategy and clinical development plans, working closely with Development and Discovery Program Leads and counterparts in Regulatory, Clinical Development, Clinical Operations, Biostatistics, Clinical Pharmacology, Medical Affairs, Commercial, Non-clinical and Discovery Research for assigned studies.
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clinical research drug development jobs Company: Us Quintiles Inc in Rockville, MD
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