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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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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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Animal handling, Animal science, Husbandry, glp, tail vein, histology, Ascp, HTL. The candidate will be a member of the Developmental and Reproductive Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
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The Post-Doc scientist will lead a research project investigating in vitro models for predictive and investigative mammalian toxicology of biotech trait proteins while considering the relationship to in vivo oral exposure for potential hazard and regulatory risk assessments.
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Bachelor's Degree in Life Science, Business Management or related field and 5+ years direct experience as a Proposal Coordinator, or similar position in the CRO, Pharma, Phase I Unit, or related life science industry, or equivalent combination of education, training, and experience.
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The candidate will be a member of the General Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection from rodents, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Minimum of 15 years in a CRO or pharmaceutical/biotech sales or operations. In compliance with goals, policies, and objectives established by the President & CEO, reporting to the CEO and responsible for the overall strategic direction of QPS clinical services.
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B.S. degree in animal science, biology or related science field with 2 years of relevant experience or an equivalent combination of education and work experience. Humane care to laboratory rodents; careful handling/restraint of animals.
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Certification as a Medical Technologist or Medical Laboratory Scientist from the American Society for Clinical Pathology (ASCP) Certification as a Medical Technologist or Medical Laboratory Scientist from the American Society for Clinical Pathology (ASCP.
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Demonstrated laboratory safety experience SLS(ASCP) certification preferred (specialist in laboratory safety) Works with departments in developing, implementing, and overseeing appropriate SH&E programs (e.g., biosafety, chemical hygiene, waste management, radiation safety and general lab safety programs.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Since its inception, 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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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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