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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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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.
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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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Plan and independently implement in vivo studies and in vivo assay development and optimization to support preclinical characterization and evaluation of targets/pathways that regulate energy balance.
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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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You will use your expertise in chromatography, spectrometry, spectroscopy, dissolution, and other established analytical methodologies to enable drug development utilizing external resources.
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Drug Safety Committee (DSC), Development Review Committee (DRC) and other. Contribute to the development of the product safety strategy and provide drug safety. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests.
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The Senior Principal Scientist role will be responsible for development and execution of drug and myeloma asset centric translational strategies in hematology for assigned programs.
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We are a leader in the development and application of computational methods to research problems in drug discovery and development, and we have extensive resources for computational support and data analysis.
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Deep understanding of the pre-clinical, translational, and clinical stages of drug development. Extensive working knowledge of biomarker and bioanalytical assay development and cutting-edge Omics methodologies in the clinic.
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The Principal DMPK Scientist is highly motivated, collaborative, and innovative with experience supporting and leading nonclinical and clinical DMPK activities to support progression of oncology based novel drug candidates into and within clinical development.
$129,500 - $191,500 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Amgen is currently seeking a talented Process Development Senior Scientist to join our Drug Substance Technologies - Synthetics (DSTS) group at Cambridge, MA. Amgen's DSTS group within Process Development (PD) is responsible for the invention and development of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets.
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Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.
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We are seeking an Analytical Development Scientist to join our Technical Operations team in Berkeley. Maintain flow cytometry and cell sorting instruments as the subject matter expert, including regular preventative maintenance, qualification, software update, data backup, SOP development, and staff training.
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The incumbent will be responsible for drug screening, cell-based assay development, and biomarker discovery. Job Description: This Associate Research Scientist will join the Translational Development Group in San Diego.
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