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This position is responsible for the development and implementation of regulatory strategies and FDA regulated quality assurance activities for pipeline programs to ensure compliance with applicable regulations (GMP, GLP, and GCP.
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Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies. Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.
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Qualifications B.S. or M.S. degree or equivalent experience in laboratory animal medicine, toxicology, animal science or biology is preferred. Adherence to good laboratory practices (GLP) is of utmost importance.
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Job Segment: Biology, Biotech, Toxicology, Pharmaceutical, Business Process, Science, Management. Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services.
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May cross-train in other areas of pathology and/or other laboratory departments (flow cytometry, clinical pathology, special pathology, bioanalytical, reproductive toxicology, etc. May cross-train in other areas of pathology and/or other laboratory departments (flow cytometry, clinical pathology, special pathology, bioanalytical, reproductive toxicology, etc.
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Superb collaborative opportunities exist with the UNMCCC Consortium partners in high-end technology and advanced material or computer sciences (at Sandia and Los Alamos National Laboratories) and GLP toxicology (Lovelace Respiratory Research Institute.
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Job Segment: Database, Toxicology, Biotech, Pharmaceutical, Science, Technology, Research. Job Segment: Database, Toxicology, Biotech, Pharmaceutical, Science, Technology, Research. Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.
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The Scientist develops, validates and implements systems, processes and procedures necessary to conduct inhalation toxicology studies in small and large animal species. Applies understanding, follows and ensures technical staff follow department and company specific SOPs, study plan requirements, GLP, A(SPA)A, USDA, data integrity Health & Safety and other regulatory guidelines.
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Job Segment: Toxicology, Database, Biotech, Pharmaceutical, Science, Technology, Research. Job Segment: Toxicology, Database, Biotech, Pharmaceutical, Science, Technology, Research. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com.
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As the Senior Scientist & Study Director, you'll provide pivotal oversight for in-vivo studies focused on cell and gene therapy, particularly in areas like Toxicology, BioDistribution, B-Cells, T-Cells, Oncology, and the Central Nervous System, primarily with immunocompromised mouse models.
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Bachelor's degree with 15 + years of scientific experience in preclinical toxicology will also be considered. Provide strategic contribution as the subject matter expert for GLP, non-GLP safety assessments, off-target risk assessment, and safety pharmacology studies supporting development and platform programs.
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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