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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
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Manages the multi-modal transportation services programs including but not limited to U-Bike, rideshare contracts, Zipcar, car pool, safe ride, and transit programs. Manages and utilizes a variety of parking management software including PaybyPhone, Genetec, T2, and other systems to for quality control, data analysis, and continuous improvement efforts to deliver service of parking and transportation needs.
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Ensure site compliance with all local, state and federal regulations including and equivalent to Federal Drug Administration (FDA), Environmental Protection Agency (EPA), Occupational Safety and Health Administration (OSHA), and Drug Enforcement Agency (DEA) as applicable (TSA) Transportation Security Administration.
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Qualifications & Experience:MD, PhD, DVM, PharmD, MBA or equivalent advanced degree of relevance, in the drug development process. Key ResponsibilitiesStrategy and Execution:Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle.
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Experience with drug development process, including affinity with clinical protocol development, global trial management, site management & monitoring, drug safety, biostatistics & programming and/or data management.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The selected candidate will manage integrated drug development projects across the full scope of the development paradigm and ensure projects are delivered on time, budget, and with high quality using proven project management decision support tools and strong leadership skills.
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Working knowledge of Food and Drug Administration (FDA), cGMPs, Drug Enforcement Administration (DEA), Occupational Safety and Health Administration (OSHA), SOPs and regulatory rules, regulations and guidelines.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Targeting 10 years of experience as lead statistician on clinical trials in the pharmaceutical industry with significant experience in rare disease drug development. Maintain thorough understanding of current regulatory guidelines and requirements relevant to rare disease drug development.
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This role involves collaboration across various teams to generate real-world evidence for drug effectiveness and disease insights using diverse data sources such as claims and electronic health records.
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Knowledge of commonly used concepts, practices, and procedures within drug discovery and development R&D laboratory settings. The Associate Scientist is responsible to conduct and/or provide support for various types of in vitro ADME assays in support of discovery and development programs in the DMPK department.
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Experience with New Jersey Department of Transportation, New Jersey Turnpike Authority, New Jersey Transit, Port Authority of New York & New Jersey, and Amtrak projects. We are looking for a technically sound environmental scientist with strong leadership skills who is ready to be challenged and lead environmental planning, documentation and permitting tasks for major transportation clients.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Interfacing with key thought leaders and experts in oncology and immuno- oncology drug development. Experience: Significant clinical research and drug development expertise and leadership experience (10 years or greater) in oncology.
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A Japan-based company, our goal is to make people smile by delivering breakthroughs where no adequate treatments currently exist, working from drug discovery to product development and commercialization.
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This position will be responsible for developing and executing robust epidemiology plans for Genmab product portfolio and pipeline in alignment with clinical development, global drug safety and pharmacovigilance and commercialization strategy.
$255,000 - $425,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
transportation drug screen jobs Title: diesel technician Company: Energy Jobline in Monmouth Junction, NJ
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