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Overview:The In vivo Associate Scientist II position will execute in vivo support for pre-clinical biomedical imaging and pathology studies toward pharmaceutical discovery and development. Studies will include rat and mouse biodistribution, disease model development, drug efficacy, and toxicology-like studies in neurology, oncology, and other therapeutic areas.
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In Toxicology, Pharmacology, Pathology, Biochemistry or Biology with extensive pharmaceutical industry experience in drug development toxicology. Conceptualizes, develops, revises, and finalizes toxicology (GLP and non-GLP) study designs and reports; drafts nonclinical sections for IND/CTA and NDA/BLA submissions and other regulatory documents.
Full-timeRemoteExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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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With annual revenues exceeding $800M and over 1000 employees worldwide, Life Sciences Mass Spectrometry (LSMS) offers customers a complete range of high-end analytical instruments and software services that support customers within proteomics, clinical research, forensic toxicology, pharmaceutical, biotech, food safety, and environmental market segments.
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Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. Responsible for safety surveillance for pharmaceutical / biological / drug -device combined early oncology products.
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Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates.
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This position will perform microbiology studies within the Formulation Development Group of at Tarrytown, NY. Main responsibilities will include execution of microbiological test methods for toxicology and pre-clinical programs, aseptic support for drug product pilot lab fill/finish operations and In-use stability studies.
$42 - $53 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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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Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. Track specimen locations throughout the laboratory workflow, including trimming, processing, embedding, sectioning, staining, distribution for QC, Pathologist evaluation, storage, and shipment.
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Bachelor's degree required in food science, microbiology, toxicology, biological sciences, or related field, preferred. Two to five years of experience in food processing or pharmaceutical environment (dairy, spray drying, or Infant Formula preferred.
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Thorough knowledge of related veterinary medical sciences such as pathology, parasitology, immunology and toxicology and /or other fields of veterinary science as required. OLAC provides a range of services, including: a) Daily animal care b) Administration of the animal health care program c) Facility maintenance d) Room monitoring e) The processing of animal and pharmaceutical orders, f) Veterinary research service support, including quarantine g) Transfer and shipment of animals h) Working with controlled substances and their disposal.
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Ensure that CRO/CMO activities and other process development activities address drug substance needs for pharmaceutical formulation development, toxicology testing, clinical trials, and commercial launch.
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The candidate is also expected to support outsourcing efforts for designing, monitoring, execution and reporting of the nonclinical toxicology studies, have experience in managing regulatory-compliant toxicology studies in a CRO or biotechnology/pharmaceutical company, and have demonstrated understanding of GLP compliance and the relevant ICH & FDA guidance documents.
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We have an exciting opportunity for a Toxicology Study Director / Pharmaceutical and Medical Device. SUMMARY The Toxicology Study Director is responsible for managing the design, execution, and reporting of studies, meeting all scientific, regulatory and client requirements.
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We are passionate about all the ways our technology can impact R&D, agricultural, and industrial applications including microbial characterization and identification, synthetic biology, bio-manufacturing, bioprocess development, metabolic and mitochondrial disorders, nutrition, toxicology, and drug discovery.
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