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Ph. D. in Genetics, Genomics, Molecular Biology or similar discipline is preferred with minimum 4 years’ post PhD qualification experience. Sampled enables clients to advance human health by leveraging active biological samples through preservation, immortalization and utilization in comprehensive multiomics research within the only leading-edge Global Integrated Analytical Biorepository.
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Experience in supporting post-approval studies/ clinical trials, including observational studies, PMR/PASS/PAES type of studies, disease/treatment registry type of studies, investigator-initiated studies/trials, and assessments of electronic health records like claims databases and preparation of health technology assessment (HTA) dossiers.
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Drive high-quality, safe, and cost-effective patient care in post-acute care communities. Drive high-quality, safe, and cost-effective patient care in post-acute care communities. Get outdoors and explore one of the areas many local parks, or enjoy boating and sailing on Raritan Bay and the Raritan River.
$260,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Must have a Bachelor’s degree in Business, Management, Engineering, Mathematics, Accounting, Finance, International Relations or a related field and 5 years of progressive, post-baccalaureate work experience applying relevant IT audit skills.
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Responsible to work on Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post-market clinical follow-up (PMCF), Summary of Safety and Clinical Performance (SSCPs), state of the art (SOTA) on medical devices, post market surveillance reports, Periodic safety update reports, Literature reviews, Protocol development, Clinical study reports, and Investigator’s brochure, Clinical Evidence Summaries, Risk-benefit analysis reports for medical devices as per MDD and MDR requirements.
$50 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Vocational or Technical Certification Post Secondary degree or Technical Certifications, Immediately hiring a Permanent Full Time Experienced Mid-Level Diesel Technician to support our Truck Fleet at Ryder in Edison, New Jersey.
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Should have awareness of changes to/ new industry regulations Have knowledge of preparation of aggregate safety reports (e.g., DSURs, Pharmacovigilance Plans,Risk Evaluation and Mitigation Strategy Plans (REMS), and EU Risk Management Plans (RMPs) Drug safety, pharmacovigilance and/or risk management industry experience in both the investigational and post-approval environments.
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Work with Contracts, legal, Presales, and Oracle NetSuite Sales team during the sale process and hand-shake information to Technology/Delivery team post sales. Work with Contracts, legal, Presales, and Oracle NetSuite Sales team during the sale process and hand-shake information to Technology/Delivery team post sales.
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Code Ninjas is the nation’s fastest-growing kids' coding franchise with over 400 open locations across the US, UK, and Canada.
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Ability to perform hand work details such as deburring and post machining details. Familiarity with the following machine controls; Fanuc, Okuma, Mitsubishi, Haas and Trak. Understanding of CNC programming and machining processes.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Earned Ph. D. degree in clinical pharmacology, pharmacokinetics, pharmacometrics, mathematics, engineering, computational biology or a related field required, with or without post-doctoral experience plus 5 years of relevant experience, OR MS/MA degree in fields listed above plus at least 12 years of relevant experience, OR BS/BA degree in fields listed above plus at least 14 years of relevant experience.
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Obtain necessary pre and post treatment vital signs and weight and perform vascular access evaluation pre- treatment. + Perform and record Pre and Post dialysis evaluation, weight, and vital signs with initial identification.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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Will handle complex cases involving alimony, child support, equitable distribution, parenting time, and other family law issues from initial interview to conclusion (including post-judgment and appeals) and other complex litigation matters.
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Our CEO, President, COO, and CNO bring a collective experience of over 80 years in post-acute care leadership, ensuring the highest quality of care for our residents. Embassy Manor has been delivering outstanding post-hospital rehabilitation, memory care, and long-term care services for more than two decades.
$28 - $34 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago
post job Title: sponsored in Dunellen, NJ
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