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Act as the lead clinical pharmacologist on clinical pharmacology study teams to support clinical development: independently lead the design, protocol development, execution, analysis, and reporting of clinical pharmacology studies (e.g., food effect, BA/BE, human ADME, drug interactions, renal and hepatic impairment, etc.
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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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Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by TFM within safety assessment. Interacts with veterinary staff, and thoroughly understands the IACUC process and the Study Director role in animal welfare.
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Interface broadly with key functions including Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late stage Clinical Research throughout sites in the USA, UK and Belgium.
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Three years’ experience as a Study Director for in vivo studies (including GLP) in a biopharmaceutical company or Contract Research Organization (CRO) One to two years’ experience in Toxicology a plus.
Up to $110,000 a yearExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Have earned at least a master’s degree in anthropology, geography, environmental education, urban studies, urban planning, sociology, public health, human dimensions of natural resources, peace studies, or a related field of study from an accredited university or college within the last 24 months and.
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Analyze and interpret study data, draw meaningful conclusions,make recommendations, and prepare comprehensive toxicology reports for clients and regulatory submissions. Key Responsibilities: Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints.
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Our client offers preclinical services for drug discovery, focused on the use of nonhuman primates to determine pharmacokinetics, pharmacology and toxicology of small molecules and biologics. 5+ years of experience in scientific sales in the Life-science industry (Toxicology, Pharmacology, Primates desired.
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The ideal candidate will play a critical role in leading and managing toxicology studies as a senior study director within CGT department, ensuring the safety of products and substances, and providing expert toxicological guidance to clients.
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Maintaining the overall schedule of nonclinical studies system to track the entire workflow of nonclinical studies and archival of study-related materials; collaborate with the Biology, Medicinal Chemistry, and CMC leads to create and maintain timelines for nonclinical studies.
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Expertise is required in the specific area of the use of animal models, humans, genetics, human immune profiling, and/or epigenetics to study mechanisms of asthma and/or allergic rhinitis causation, airway injury and aberrant lung repair due to environmental exposures.
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Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT)? Your New Chapter Awaits:As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe.
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QPS’ Story: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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Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies. Your Credentials: 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.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Toxicology and epidemiology systematic review tasks, including literature screening, study quality evaluation, and study data extraction. A bachelor’s degree in toxicology, epidemiology, pharmacology, environmental science, or another related subject.
Part-timeExpandUpdated 17 days ago
toxicology study jobs
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