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Faculty Rank or Job Title Research Apprentice (3 positions) Job Category: Research Department Pharmacology & Toxicology-SOM EEO number: 24P168 Position FTE. Faculty Rank or Job Title Research Apprentice (3 positions) Job Category: Research Department Pharmacology & Toxicology-SOM EEO number: 24P168 Position FTE.
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One year of Pharmacology/Toxicology experience is preferred. In Vivo Research Associate I position is to provide support on In Vivo studies within the In Vivo Pharmacology group meeting the Company's goals, objectives, and quality standards.
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Environmental Toxicology and Pharmacology i. Demonstrate a commitment to pursuing a Ph. D. or career in a biomedical science or cancer research field. Requisition ID req27690 Working Title Research Assistant/Staff - PREP Scholars Position Grade 06 Position Summary.
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Strong working knowledge of biochemistry, biophysics, ADME, pharmacokinetics, biology, pharmacology, DMPK, and toxicology. Head of Medicinal Chemistry and Head of the Novo Nordisk (NN) Small Molecule Research Unit. Will interact and closely collaborate with other Small Molecule Unit Scientists (chemists, biochemists, biophysicists, crystallographers), Data Science & Innovation (DSI) computational chemists, Global Drug Discovery (GDD) biology, Global Research Technologies (GRT), GDD Drug Metabolism and Pharmacokinetics (DMPK), cellular biology, pharmacology and translational medicine teams globally.
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7 or more years of experience within pharmacovigilance, clinical pharmacology, preclinical research, toxicology and/or biomarker validation (especially in industry) required. Grow CSPV’s connection to toxicology (MSRL) and Precision Medicine beginning at the start of preclinical development.
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PhD or MSc (with equivalent experience) in a relevant field (e.g., Biology, Biochemistry, Pharmacology, Toxicology, Engineering, Physics) Hands-on experience establishing and optimizing in vivo pharmacology models and assays.
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Provide thorough understanding of pharmacokinetics, pharmacology, toxicology, drug design, use of in silico tools, ability to interpret in vivo results, drug discovery process, purification techniques, and ability to analyze target compound spectra obtained by analytical instruments to characterize compounds such as nuclear magnetic resonance (NMR), infrared spectrometry (IR), mass spectrometry (MS), and elemental analysis.
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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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This position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical pharmacology and toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial.
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Manage effective cross-functional collaboration, especially with in vitro/in vivo pharmacology and toxicology and provide guidance in the optimization of drug leads and candidates, in understanding of PK/PD and human dose projections.
$173,000 - $230,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Job DescriptionTakeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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The tenure-track faculty member will also be expected to teach pharmacology and/or toxicology to professional and graduate students and promote the development of the department through other forms of service supporting ECU's commitment to student learning and regional transformation.
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Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. The PST lead will also closely collaborate with a PK and toxicology leads to help guide dose selection and regimen, inclusion/exclusion criteria and safety monitoring for first in human and phase I/II studies.
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Takeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Administrative Associate 2 conducts advance-level administrative duties for the Department of Pharmacology, Addiction Sciences and Toxicology (PHAST) to include providing complex and confidential support to the faculty, staff, and customers of the department.
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