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Strong tactical familiarity with the design, overseeing and assessment of clinical trials and with other medical affairs activities (expertise in clinical trial methodology and conduct, GCP principles, medical product support activities, publications, ISS, continuing medical education.
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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The Position The Rapid Cycle Analytics (RCA) Lead Data Scientist role sits within the Clinical Data Science and Evidence (CDSE) team, which is part of CMR. This role interfaces with internal stakeholders from Health Economics and Outcomes Research (HEOR), Real-World Evidence (RWE), Medical Affairs, Clinical Trials Operations, Market Access, and a few other teams to respond to quick turnaround data analytics requests.
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Designs and develops clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies.
$308,000 - $354,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reports to the Executive Director- Clinical Research & Development. Prior clinical research or related experience (e.g. monitoring of clinical studies, knowledge of drug development phases, statistical research methodology experience.
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For more information on our company, our brands and our culture visit us at Category:Marketing & Biz Dev, Keywords:Market Research Manager, Location:EWING, NJ-08629. This Market Research Manager collaborates across the Data & Analytics Office to provide the Commercial (Brand & Sales) and New Product Teams guidance & insight based on a solid understanding of the consumer for assigned categories.
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Dr. Jennifer Pacyon, co-director of the training program, brings a broad range of forensic and clinical experience to the program with a particular specialization in pediatric neuropsychology and forensic psychology.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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3-6 years of experience in Clinical Research Associate (CRA) tasks, including remote monitoring, SOP creation, site selection setup, and protocol development. Position Summary: The Senior Clinical Research Associate (Sr. CRA) will be responsible for overseeing and executing various clinical research activities, including remote monitoring, protocol development, site selection and setup, and SOP creation.
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Oversee a coherent and cogent agenda for the development and execution of interdisciplinary research programs described above which are conducted by ETS scientists who work — often in collaboration with researchers at universities and institutions from around the world — in disciplines that include statistics, psychometrics, educational research, cognitive science, psycholinguistics, AI, computer science, and public policy.
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The molecular genomics Sr. Scientist role is responsible for developing molecular assays and generation of research use genomics data in support of BMS clinical trial analysis. This includes but is not limited to responsibility for genomics and gene expression profiling (GEP) biomarker assay technology/ platform selection, evaluation of in-house or vendor choice per assay use requirements, development, optimization, qualification/validation and/or execution of biomarker analysis for BMS translational medicine and clinical programs.
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Our Market Access and Public Affairs professionals ensure that the latest therapies and products reach the people who need them most, by creating an environment where innovation and chronic disease management drive optimal health outcomes.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Establish procedures to record in Altru: all research, peer prospect review, and solicitation notes on prospects and donors; and gift strategies and activities. Committed to advancing the University’s teaching and research missions, the Museum also serves as a hub for the humanities at Princeton for visitors worldwide.
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Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program. Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required.
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clinical research affairs jobs Title: director Company: Biophase in Princeton, NJ
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