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In this Scientific Senior Director role you will lead a team that is responsible for driving the neuroscience portfolio by providing platforms and technologies that be utilized for target validation, biomarker identification and supporting SAR in drug discovery programs.
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Our staff in Epidemiology provide leadership and expertise to develop and execute the Epidemiology strategy across the entire spectrum of drug development, from early drug discovery to registration and lifecycle management.
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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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Approaches to accelerate drug development using high dimensionality data (e.g., high content imaging, transcriptomics and proteomics data) combined with advanced analytics. value of human data in precision drug development including molecular datasets and human cell models.
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Discovery Pharmaceutical Sciences (DPS) is a multidisciplinary research group that enables drug discovery and drug product development through application of pharmaceutical science to drug delivery research from target identification through clinical candidate selection for both small and large molecules as well as vaccines.
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Coordinate with advanced analytics and machine learning teams to use knowledge graph for insights, predictions, and innovation in drug discovery and development. This team focuses on building innovated data products and solutions for the entire drug discovery and development value chain: from target ID/Validation, molecule design, product development, clinical trial design, digital end points, clinical trial operations, and using real world data to advance our portfolio.
$135,000 - $202,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The scope of responsibility spans drug discovery and development, medical affairs, marketing and brand management, sales, managed markets, manufacturing operations, trade and distribution, and finance.
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Collectively, the team is accountable for CMC activities encompassing cell line development, cell culture/ microbial fermentation, purification development, and drug product/ device development.
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Reporting directly to the Analytical Development (AD) and Testing Lead, the Analytical Development (AD) and Testing Senior Analyst will support the management of the life cycle of analytical development for in-process, release and stability program testing of raw materials, plasmids, cell/bacterial banks, drug substance and drug products, in support of discovery, development, and manufacturing of iECURE’s product portfolio from the clinic through commercial launch.
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Experience in scientific disciplines related to drug discovery and development, including biology, chemistry, toxicology, and pharmacology. Experience in the development and application of computational approaches in drug discovery Experience in leading teams Preferred Qualifications: If you have the following characteristics, it would be a plus: Experience in leading teams that positively impacted progression of the discovery portfolio via leading in a matrix setting at all levels and leveraging Subject Matter Experts to define standards and ensure fit for purpose solutions.
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You will be able to anticipate, communicate, and suggest solutions on trends/events outside GSK that affect our business direction - utilizing command of the drug discovery and development process to influence a culture of continuous improvement.
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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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Executes drug product development and commercialization studies, new product introduction and process validation at the commercial site. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
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A minimum of 8 years related experience in drug development, including target discovery and validation is required. Experience in advancing biologics from early discovery to clinical development is required.
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