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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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This includes organizing, assigning, and overseeing key preclinical and clinical experimental projects in support both compound specific programs and on broader clinical translational research scientific projects.
$142,500 - $237,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Prior clinical research or related experience (e.g. monitoring of clinical studies, knowledge of drug development phases, statistical research methodology experience) Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs, Regulatory Affairs and other NNI skill areas.
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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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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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5+ years of experience in health economics, outcomes research, pricing, reimbursement, medical affairs, and/or portfolio analysis, preferably with at least 2 years in the pharmaceutical industry.
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Caseload of clinical evaluation and treatment cases of patients with mild TBI, PTSD and other accident-related disorders, to include psychotherapy, biofeedback and cognitive rehabilitation under supervision.
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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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Ensure that research programs are conducted to meet those scientific, professional, and ethical standards. Participate in discussions on key organization-wide strategic issues and ensure that scientific staff are working effectively with external clients, strategic business units, and ETS functional centers of excellence to inform their work on research and emerging issues.
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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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Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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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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Genmab is seeking a highly skilled Senior Contract Manager specializing in nonclinical and clinical lab and data services to join our team in Research & Innovation Outsourcing Management.
$95,625 - $159,375 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical research scientific affairs jobs Company: Biophase in Princeton, NJ
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