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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.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Safety or occupational health fields (safety, occupational health, industrial hygiene), or degree in other related fields that included or was supplemented by at least 24 semester hours of study from among the following (or closely related) disciplines: safety, occupational health, industrial hygiene, occupational medicine, toxicology, public health, mathematics, physics, chemistry, biological sciences, engineering, and industrial psychology.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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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Experience in animal husbandry/in-vivo study conduct within Toxicology strongly preferred. Kelly® Science & Clinical is seeking In Vivo Study Monitor for aposition at a Biotech company in Thousand Oaks, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Serves as Study Director on toxicology, biodistribution, pharmacokinetic, and related studies to ensure study execution, client engagement, and deliverables upon study completion.
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Researching, organizing and assimilating clinical, safety, and/or toxicology information to support medical safety assessments, clinical study related safety reports, safety fact sheets and chemical approvals.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Serves as Study Director, Contributing Scientist/Principal Investigator (providing expertise in electrocardiography, cardiovascular, respiratory, or central nervous system subject matter), on pharmacology or toxicology studies according to the protocol/study plan, Standard Operating Procedure(s), and to the highest possible scientific standards.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Minimum of 10 years of experience as a regulatory toxicologist (study director/monitor and/or project lead) in the pharmaceutical or biotechnology industry or within a regulatory authority. Advanced knowledge of toxicology, pharmacology, safety pharmacology & DMPK.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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The Study Technician provides primary care to the animals in the small and large animal toxicology department and performs routine invasive and non-invasive technical procedures on studies allocated to the team while ensuring that procedures are conducted according to protocol, SOP requirements, Good Laboratory Practice (GLP) and United States Department of Agriculture (USDA) regulations and the guidelines The Guide for the Care and Use of Laboratory Animals.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Responsibilities include establishment of, and adherence to, non-clinical study timelines, monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ADME/ToxPath/Drug Disposition (ATP) team throughout study planning, execution and reporting.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe. Associate Director, Toxicology - Cell & Gene Therapy. Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies.
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Shown technical writing ability and oral presentation to enable clear communication of study results, safety evaluations, and toxicology assessment conclusions. The role will report to Associate Director of Preclinical and Toxicology assessment and will be part of a global team responsible drugs and devices for Peritoneal dialysis, Hemodialysis, and Acute therapies (~$5B product portfolio with global reach in more than 100 countries.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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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Ph. D. in Toxicology, Pharmacology, or a related field. Your expertise will guide critical toxicology studies from conception to conclusion, ensuring excellence and integrity at every step.
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toxicology study jobs
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