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This position will work in close collaboration with different functions, including preclinical toxicology, preclinical pharmacokinetics, translational medicine, clinical, operations, and regulatory affairs.
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Option 3:A Ph. D. with major study in environmental science, toxicology, organic chemistry, hydrology, geography, oceanography, limnology, aquatic science, fish ecology, or other closely related natural science field.
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Leaders in their fields, the School includes fellows of the National Academy of Kinesiology, the American Statistical Association, the Human Factors and Ergonomics Society, the American Academy of Health Behavior, and the Society for the Scientific Study of Sexuality.
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Analyze and interpret study data, draw meaningful conclusions,make recommendations, and prepare comprehensive toxicology reports for clients and regulatory submissions. Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints.
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Key Responsibilities: Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints. Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout. Working knowledge of all functional areas of exploratory development, including chemistry/biochemistry, biology, toxicology, CMC, translational medicine, early clinical development, regulatory, etc., and demonstrated ability to successfully and effectively cooperate, collaborate and work across functions.
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In addition, a laboratory manager will be required to have the critical thinking skills pertaining to the optimization of assays, mentoring abilities towards undergraduate and junior graduate students, active participation in study design, execution, analysis, and presentation of scientific data.
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The Senior Scientist functions as a study director to manage the design, execution, analysis, and reporting of pre-clinical discovery research studies across various therapeutic areas. The Senior Scientist is expected to deploy their scientific domain expertise to 1) lead communications with sponsors, 2) interface with business development teams, 3) engage laboratory staff and IACUC, and 4) coordinate with project management and data analysis teammates to manage all aspects of studies from initial pre-clinical study design to final report.
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Position/Job Summary: The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines.
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Provide scientific and administrative leadership to a growing organization with particular strength in preclinical toxicology, cancer prevention and therapy, and infectious disease. Serve as Principal Investigator/Study Director for programs conducted for commercial and government sponsors.
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Oversees the QA reviews of GMP manufacturing batch records, product release and stability testing, validation reports, pharmacology and toxicology study reports and essential clinical study documents.
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Scientific expertise in one or more technical areas of ADME, Toxicology, and DMPK such as bioanalysis, solution properties testing, in vitro metabolism, in vitro absorption, in vitro Toxicity assessment and metabolite ID.
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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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Managing 3M databases and documentation for toxicology study archival and retrieval. Coordinating toxicology study placement with internal 3M Strategic Toxicology Laboratory, as well as with 3rd party contract research organizations.
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You have at least 5-10 years experience as a study monitor and/or study director conducting non-GLP and GLP toxicology studies, e.g. as Study Director at a CRO or in a pharma company.
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toxicology study jobs
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