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Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Posting Summary There are two postdoc positions available in Dr. Shuo Xiao’s lab at the Department of Pharmacology and Toxicology, Environmental and Occupational Health Sciences Institute (EOHSI)/Ernest Mario School of Pharmacy, Rutgers University.
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This position is in the Translational Medicine and Clinical Pharmacology department at Sanofi that covers Rare Diseases, Rare Blood Disorders, and Genomic Medicines with a scope that includes small molecule, monoclonal antibody, peptide, nucleic acid, and genomic therapy modalities.
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Job Summary:The Senior Director, Quantitative Systems Pharmacology (QSP) will work within the Quantitative Clinical Pharmacology (QCP) group to develop and apply QSP models to aid in target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design.
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This position will be part of the Quantitative Clinical Pharmacology (QCP) team and support drug development and commercialization activities. It is accountable for the Clinical Pharmacology and Model-Based Drug Development (MBDD) plans and deliverables.
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Legend Biotech USA, Inc. is seeking an experienced senior in vivo pharmacologist to join our in vivo pharmacology team responsible for conducting in vivo studies with mice and NHP to support pipeline development.
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These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services Project Management and Operational Management.
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Provide excellent pet care by applying full knowledge of anatomy, physiology, disease processes, pharmacology, specialized equipment usage, and specialized drug administration. Certified Veterinary Technician (CVT), Licensed Veterinary Technician (LVT), Registered Veterinary Technician (RVT), or the Licensed Veterinary Medical Technician (LVMT) preferred or as required by State.
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Assist in the design and authoring of clinical pharmacology study protocols (e.g., food effect, PK, human ADME, drug-drug interactions, TQT, and hepatic/renal impairment). Draft and review relevant clinical pharmacology sections in clinical study protocols, PK analysis plans, study reports, IBs, INDs, NDAs, etc.
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Develops formulations for compounds from drug discovery and clinical phase development programs for evaluation in pharmacokinetic (PK), efficacy, and other pharmacology studies; develops formulations that enable the delivery of water insoluble compounds in preclinical and clinical studies by providing safe and viable formulations composed of pharmaceutically acceptable vehicles and excipients dosed by multiple routes of administration.
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It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
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4 or More Years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug.
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Solid working knowledge of pharmacokinetics and modeling, PKPD principles, ADME concepts, and clinical pharmacology. The clinical pharmacologist will be responsible and accountable for designing clinical pharmacology programs and studies, performing PK and PKPD data analysis, supporting clinical dose selection and authoring summary and regulatory submission documents.
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The Senior Principal Scientist CPP Leader is responsible and accountable for developing compound specific Clinical Pharmacology strategy for the development of a compound, including interactions with regulatory agencies and functions as CPP Leader on the Compound Development Teams (CDT) working in collaboration with various stakeholders within the team and within Quantitative Sciences (e.g., Statistics, Pharmacometrics.
$267,145 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Bachelor's Degree Chemistry, Chemical Engineering, Biology, Biochemistry, pharmacology or Organic Chemistry. Focused on Oral Care, Personal Care, Home Care and Pet Nutrition, we sell our products in more than 200 countries and territories under brands such as Colgate, Palmolive, elmex, hello, meridol, Sorriso, Tom’s of Maine, EltaMD, Filorga, Irish Spring, PCA SKIN, Protex, Sanex, Softsoap, Speed Stick, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Pet Nutrition.
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pharmacology job in Bridgewater, NJ
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