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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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Knowledge of: Principles and practices of modern medicine and techniques of autopsy; statues, ordinances, regulations and medicolegal issues related to Coroner's Bureau; the current and highly specialized techniques, investigative procedures and equipment applicable to forensic pathology including the applicability of toxicology, ballistics/firearm examination, trace evidence, forensic serology, forensic anthropology, and DNA technology; rules and regulations applicable to court testimony.
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As an Assistant Administrator and Forensic Toxicology Expert, I serve as a consultant and supervisor for the military drug testing community and the Armed Forces Medical Examiner. Act as a consultant and assistant contractor supervisor/administrator to the military drug testing community and the Armed Forces Medical Examiner, providing expertise in Forensic Toxicology.
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As a Staff Scientist I in TLM, you will be a key contributor in a laboratory role focused on the analysis of drug or other targets in complex biologic matrices using immunologic methods. Please visit our careers page to see other positions ranging from entry-level analyst to Research Scientist and Team Lead.
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Interface broadly with key functions including discovery sciences, preclinical development groups, toxicology, clinical operations, drug metabolism, regulatory affairs, and late-stage clinical research.
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Our client 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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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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Generate Request for Proposals (RFPs) from new clients for QPS' small molecules, biotherapeutics (proteins, gene therapy, and cell therapy), non-GLP Bioanalysis and Preclinical (DMPK) services. As part of a dynamic team, BD plays a critical role in identifying areas of growth, and aligning our DMPK, Bioanalytical and Preclinical offerings with the current trends in drug discovery and development.
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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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Proficiency in murine handling techniques handling and restraint, assessment of clinical signs, IV, IP, PO, ID, SC in life and terminal blood collection, and handling of tissues during necropsy and processing for ex vivo analysis is critical for this role.
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Experience with clinical trial process, clinical drug development and approval processes. Assist in creating and revising CRS department applicable SOPs. Provide consultation to clients on drug development process, strategy, and plans as needed.
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Graduation from an accredited college or university with a Master's degree in Aquatic Biology, Wildlife Biology, Fisheries, Zoology, Ecology, Natural Science, Environmental Science, Ecotoxicology, Environmental Toxicology, or closely related field may substitute for one year of the required experience.
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III. A Graduate degree with a major in environmental science, biology, chemistry, earth science, environmental health, meteorology, natural science, toxicology or public health may be substituted for a maximum of three years of the required (A) experience and one year of the required (B) experience.
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Development and execution of early clinical strategy for novel therapeutics including authoring initial clinical biomarker plans, early clinical development plans, and clinical pharmacology studies for programs in Phases I through IV of development.
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15 years relevant work experience in clinical pharmacology and project management in a function as Clinical Pharmacologist, Scientist, Research Physician or a comparable function in clinical research.
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