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Collaborates with NPM's staff across Clinical Science, Digital Health, Software Engineering, Data Science, and Informatics to detail AI model functionality and requirements to significantly increase efficiency in the areas of document control, clinical information extraction, information synthesis and clinical note preparation.
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Assist the Division Counsel for Research in the review of and advice on research enterprise concerns, including effort reporting, grant accounting, clinical trials billing, and the application of the fraud, waste and abuse laws and regulations to sponsor-supplied equipment, medication and treatment supplies.
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The primary role for this Protocol Navigator (PN) position is to provide clinical research regulatory support through the NINDS Clinical Trials Unit (CTU) for the NINDS Intramural Research Program, including specific groups as assigned.
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We are seeking a Biostatistician 3 to facilitate cutting-edge scientific studies initiated by investigators at Byers by providing expertise in biostatistics and informatics, including mentorship and education for clinical investigators in research methods.
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The Platform fully centralizes RWE, epidemiology, outcomes research, RW-relevant health informatics, and biostatistics talent from global, international developed market (IDM) and emerging markets (EM) into one team to drive efficiency through internalized work.
$262,100 - $436,800 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Outside of the Platform, the Head will work with leaders from Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HEOR, Legal/Compliance, and others to achieve research and business objectives.
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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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The Chief Medical Affairs Office's Evidence Generation (EvGen) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept (POC) trials through LOE for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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A blend of non-pharmaceutical (academia, government, NGO) and pharmaceutical experience in relevant areas for target assets; pharmaceutical experience could be through partnerships or engagement in sponsored trials/studies rather than through employment.
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Advocate and champion for the science and clinical value of Pfizer's pipeline & products within the target asset classes and for transformative policy changes to increase global regulatory agency, patient and provider confidence in and acceptance of RWE.
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The RWE Science & Epidemiology capability is the primary execution arm of the EvGen Platform for retrospective RWE generation using retrospective RWD sources or technology-based direct-from-patient approaches for observational, hybrid interventional / RWE trials and other approaches.
$262,100 - $436,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In conjunction with the CIO, serve as the primary liaison to the Office of Research, Health Transformation Research Institute, and Biomedical Data Science Hub on institutional-level matters regarding technology and infrastructure, specifically including needs associated with clinical trials and clinical research.
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Architecture Development, Architecture Development, Architecture Management, Biochemical Analysis, Biochemical Assays, Biochemical Tests, Bioinformatics, Biology, Biopharmaceuticals, Biotechnology, Cell-Based Assays, Cell Biology, Cell Physiology, Chemical Biology, Clinical Trials, Computer Science, Data Architecture, Data Integration, DNA Microarray, Immunoassays, Immunochemistry, Immunology, Information Architectures, IT Project Lifecycle, Laboratory Informatics {+ 9 more.
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The research portfolio of the department is broad and well diversified including focus areas in addiction medicine, geriatrics, implementation science, clinical informatics, health services research, critical care clinical trials, and health equity.
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The Platform: The Chief Medical Affairs Office's Evidence Generation (EvGen) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept (POC) trials through LOE for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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