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The Director will develop collaborative partnerships with the cross-functional Insmed team (Medical Affairs, HEOR, Clinical Development, Advocacy, Commercial and Market Access) as well as external medical experts and will have an integral role in driving the planning and execution of scientific communications deliverables across the Insmed respiratory franchise.
$250,800 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The Scientific Knowledge Engineering team, which sits within the Onyx Product Management organization, is responsible for the data modeling, ontology definition and management, vocabulary mapping, and other key metadata activities that ensure Onyx platforms and data assets speak scientific language.
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Are you looking for an opportunity to utilize your scientific background and clinical expertise to support new product innovation, research, and generation of consumer claims and communications to promote everyday health and wellness.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Related fields include Health Services Research/ Outcomes Research/Health Economics, Economics/Econometrics, Pharmacoeconomics, Public Health-Health Policy & Management, Epidemiology, Psychometrics, Statistics/Biostatistics, Pharmacy Administration.
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The ideal candidate will have a proven track record of conducting clinical research studies, with a focus on conducting oral health clinical trials. The candidate must have 4+ years of clinical research experience (design, implementation, and analysis of randomized controlled trials.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Summarize experimental results and present scientific findings at both internal and external research meetings. Specifically, the candidate will support the development and optimization of pre-clinical and clinical assays for neutrophil-mediated diseases by assisting with cell culture, in vitro and ex vivo assays, and molecular biology assays.
$90,467 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Expert in HEOR research including burden of illness studies, patient evidence studies, medical claims and electronic health records database analyses, economic models, and systematic literature reviews, analytic methodologies and modeling, scientific data interpretation and presentation.
$241,667 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Ability to address complex scientific problems with practical research plan and efficiently execute and A proven record of making critical scientific decisions and demonstration of a thoughtful and decisive approach.
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New Jersey's academic health center, Rutgers Biomedical and Health Sciences (RBHS) takes an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health.
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Bachelor's degree in a relevant scientific discipline and United States Patent & Trademark Office (USPTO) Registration as a Patent Attorney. Accountable for collaboration with cross-functional teams, including research and development, legal, regulatory affairs, and business development, to ensure IP considerations are integrated into product development and commercialization strategies.
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To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Associate Director, Statistical Programming for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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The Scientific Director, US Medical Affairs, Endocrinology will serve as a scientific/medical expert to lead and manage strategic initiatives and projects that integrate Recordati’s scientific, clinical data into programs that drive business and medical affairs priorities.
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7 or more years of experience within pharmacovigilance, clinical pharmacology, preclinical research, toxicology and/or biomarker validation (especially in industry) required. Surface expert knowledge on safety biomarkers that might be used in preclinical and clinical development by closely collaborating w Research and Precision Medicine.
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Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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This individual will be responsible for delivering CMC documentation (Dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application.
$41.8 an hourExpandApply NowActive JobUpdated 20 days ago
clinical research scientific jobs Title: director Company: Biophase in Bridgewater, NJ
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