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Pharmaron is a premier contract research organization that offers a broad spectrum of R&D and manufacturing service capabilities throughout the entire drug discovery, preclinical, clinical development and commercialization process.
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Quality Control Specialist-Large Molecule Exton, PA (Corporate) Frontage Laboratories 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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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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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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The Center for Immunobiology, Center for Clinical Research, Research Histology Lab, Innovation Center, and Human Research Protection Program contribute to the medical school’s advancement of knowledge through innovation and discovery.
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The incumbent will be responsible for drug screening, cell-based assay development, and biomarker discovery. Work at the bench to develop and execute established and Client molecular and cell-based assays for drug screening as well as understanding molecular pathways (Proliferation, Apoptosis, Flow Cytometry etc.
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Familiarity with and exposure to drug discovery and clinical development processes with one or more of the following therapeutic areas: oncology, immunology, cardiovascular, neuroscience, pulmonary hypertension, or infectious disease.
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A recent or almost completed Ph. D. degree or equivalent experience in a quantitative field (e.g., statistics, biostatistics, epidemiology, artificial intelligence, computer science, operations research, industrial & systems engineering, applied mathematics, health economics, biomedical informatics, or similar.
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Perform techniques such as cell culturing, preparing samples for live-cell microscopy, mesoscale analysis, flow cytometry, molecular biology procedures, and testing drug regimens. perform techniques such as cell culturing, preparing samples for live-cell microscopy, mesoscale analysis, flow cytometry, molecular biology procedures, and testing drug regimens.
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The Manufacturing Associate I/II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics' multiple clinical programs in the Protein Purification area. MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies.
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Discovery Biotherapeutics at AbbVie is seeking a highly-motivated research scientist to join a dynamic team supporting biologics drug discovery. The ideal candidate has direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry.
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The role involves contributing to innovative approaches in evaluating the ADME of therapeutic proteins, peptides, and new modalities like RNbased therapeutics and antibody-drug-conjugates. Serving as the Bioanalytical Project Lead for discovery projects requiring input from a highly qualified scientist on issues related to PK/PD and biotransformation.
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As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry.
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AnTolRx, Inc. is seeking a highly motivated Scientist/Senior Scientist to join its research team in Cambridge, MA. The ideal candidate has a strong background in lipid nanoparticle formulation and drug delivery, is a self-starter, and is looking to make a significant impact on our cross-disciplinary team.
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Bachelor's degree in a scientific discipline relevant to drug discovery, development, pharmacy, biology, or chemistry and a minimum 3+ years' experience in pharmaceutical or medical device manufacturing quality assurance with at least 3+ years' relevant to parenteral product aseptic processing.
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