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Frontage Laboratories is a CRO / Clinical Research Organization providing integrated, science-driven, product development services throughout the drug discovery and development process to enable life science companies to achieve their drug development goals.
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Apply knowledge in protein biochemistry, biophysics and mammalian cell biology to support drug discovery at ViiV. Engage and network with scientific leaders in drug discovery across ViiV R&D.
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Drug discovery knowledge, biopharma CRO and relevant business experience required. GemPharmatech is a global company providing high-quality products and model systems for preclinical discovery, testing, and development of new drugs and therapeutic solutions.
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The Vice President of Business Development will engage with pharmaceutical companies and hospitals to commercialize Pear Bio’s precision medicine platform and drug discovery pipeline. Our patient data, biobank and biomarker technology have led to the creation of an in-house drug discovery pipeline for cancers with high unmet need.
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Ph. D. with minimum of 15 years of working experience, including proven track record in the discovery and development of drugs for diseases of peripheral tissues/organs in the pharmaceutical and/or biotechnology industry, substantiated by publications, patent filings, and/or other, from tenure in drug discovery and development as characterized.
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The successful candidate is a confident leader with extensive prior success in drug discovery, preferably in multiple therapeutic areas such as immunology, oncology, metabolic diseases, CNS, etc.
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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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We are seeking a skilled, motivated, and versatile individual who can help build a highly collaborative, successful drug discovery and development team in the Obesity Research group in Cambridge.
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The successful candidate will use their strong in vivo pharmacology background and complementary laboratory skills to support discovery efforts and established pipeline projects with an emphasis on anti-obesity therapeutics.
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Perform various molecular and biochemical assays on tissue samples from preclinical in vivo studies for early discovery drug development programs, including quantitative and qualitative analysis of target mRNAs and proteins (tissue homogenization, RNA extraction, Western blot, ELISA, qPCR, dPCR.
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As an in vivo pharmacologist, they will integrate with Discovery project teams and work closely with medicinal chemists, drug discovery and translational biologists, DMPK, and data scientists to validate therapeutic hypotheses in vivo, build PD-PK-efficacy relationship, identify lead series and nominate candidates, and enable the identification of lead target indications and translational strategies.
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Act with leadership of drug discovery efforts contributing to drug development pipelines in immunology. Principal Investigator of Immunology, Therapeutics, Large Molecule, Flow Cytometry, In Vivo, In Vitro, Western Blot, ELISA, PCR, Research, Science, Comprehensive Benefits Package, Health, Vis, Dental.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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WMed is building upon Kalamazoo's century-long foundation of drug discovery and medical device development with a strategic investment in clinical, laboratory, community, and educational research.
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For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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