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In this role, a typical day might include:The Regulatory Intelligence Manager performs proactive global monitoring and surveillance of changes in the regulatory landscape focused on the drug development lifecycle, i.e., preclinical through commercialization, as well as disseminate relevant regulatory intelligence information to Regeneron stakeholders.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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Act as the project manager to support the externalization and operationalization of clinical biomarkers and bioanalytical activities for pre-clinical and clinical drug development. Must have Bioanalytical experience so they can help lab troubleshoot issues when applicable, Outsourcing experience preferred but the major focus/must haves should be at least years (with masters or higher degree) or years (with bachelors degree) bioanalytical experience, regulated experience, experience supporting clinical studies, biomarker ops or analysis.
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Locally great and nationally strong, Albertsons Companies (NYSE: ACI) is one of the largest food and drug retailers in the United States. The organization includes 2,273 retail and drug stores with 1720 pharmacies, 402 associated fuel centers, 22 distribution facilities, and 19 manufacturing plants with over 300,000 employees across 34 states and the District of Columbia.
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Demonstrate excellent customer service and customer interaction (via phone, e-mail and face to face) Qualifications High School diploma or GED required Background investigation and drug screen required Experience working with A/V and teleconferencing / videoconferencing systems.
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The Pharmacometrics Group applies a range of model informed drug development (MIDD) approaches to support early and late-stage development of small and large molecules. Top Tier BioPharmaceutical company looking to add a Principal Scientist to their dynamic Pharmacometrics team.
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The company maintains a drug-free workforce, including post-employment substance abuse testing pursuant to a Drug and Alcohol Policy. Under direction of the Creamery Supervisor and other Work Center 1 leadership staff, the Cheesemaker is responsible for assisting in pasteurization and cheesemaking processes.
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Collaborates with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy. Demonstrated expertise around the lifecycle of oncology drug development with ability to strategically analyze oncology clinical trial protocols.
$261,200 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This position also contributes to drug product development and life cycle management by designing and developing formulations and processes for preclinical & clinical evaluations as well as for commercial technology transfer.
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Job title: Global Regulatory LeadLocation: Bridgewater, NJ or Cambridge, MAAbout the job:Our team is involved in developing regulatory product strategies for the Immunology and Inflammation therapeutic area, leading regulatory efforts in the development stage of drug products.
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We are proud to be an EEO employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. This is a full-time position working 11AM-7PM at our Bridgewater, NJ outpatient eating disorder program.
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Leads the task of establishing study-specific work procedure for reporting Anti-Drug Antibody data from bioanalytical lab to clinical sites. Manages memberships, facilitates meetings to assemble study deliverables at multiple decision points in the Global Drug Development Process and authors meeting summary across multiple PrM sub teams.
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In the United States we are proud to be an EEO employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. Greeting and seating guests and controlling the flow of guests coming into the restaurant, bar and lounge while under pressure.
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Excellent understanding of the overall drug development process, including its various development phases, such as pre-clinical development, clinical development, regulatory development, and commercialization is an absolute must.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Must Submit to a background check and drug screen. Weekly Pay and Immediate Start Position Summary: Will accurately and efficiently prepare, portion, cook, and present a variety of hot and/or cold food items for various meal periods to include: Breakfast, Lunch, Dinner, and Special/Catered Events.
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drug job in Peapack And Gladstone, NJ
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