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We work in an exciting, interdisciplinary environment and collaborate with multi-functional teams, including biologics discovery, cell line development, analytical sciences and cell culture process development.
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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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The J&J IM Discovery, Product Development, & Supply (DPDS) Postdoctoral Fellowship Program helps early career scientists gain the training and experience needed to further their careers while addressing the needs of global healthcare.
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Like the communities we serve, you are on a constant path of discovery to shape your career and personal development. With our range of services, including landscape design, development, maintenance and enhancements, there’s no limit to what we can do, and what you can achieve.
$85,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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High level of proficiency in Consolidation ERPs (Oracle and OneStream a plus) and Excel to perform spreadsheet and financial analysis. Provide training and coaching to Branch teams and supports the VPGM & Regional VP Finance.
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Work collaboratively with functional partners including Clinical Development, Biostatistics, Discovery, Translational Medicine, CMC, Toxicology, DMPK, Clinical Operations and Regulatory to deliver on project and corporate objectives.
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Growth and Development: Business Resource Groups | Tuition Reimbursement | Professional Development. Just like uncovering a delightful find in our stores, there is potential for discovery and fulfillment in every job at Cracker Barrel.
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In-depth knowledge and understanding of the drug discovery and drug development processes. Strong knowledge of key pharmaceutical functions throughout all stages of product development, including Marketing (e.g., Market Research, Market Access), HEOR, Medical Affairs, Preclinical, Clinical, Regulatory, CMC (e.g. supply chain, drug delivery), etc.
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You will work closely with our Data Science colleagues to leverage large data sets e.g. proteomics and transcriptomics, as well as genetic and real-world evidence data to shape the discovery portfolio.
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We can accomplish our mission by building deep expertise in large molecule end-to-end discovery such as Antibody discovery, protein engineering and optimization, molecular attribute characterization, target protein & expression sciences, and platform biology/in vitro pharmacology/assay development.
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Working with the Asset Development Team (ADT's), early- & late-stage clinical development teams, the Biomarker (BMx) leads will develop asset-specific clinical biomarker strategy by incorporating critical insight from discovery biology, clinical development, diagnostics, bioinformatics, molecular assay experts, Quantitative Pharmacology Pharmacometrics (QP2) and Biostatistics and Research Decision Sciences (BARDS.
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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. Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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The individual selected to fill this position will be expected to support the bioreactor sampling and feeding of cell lines expressing therapeutic proteins within the Cell Line Development group.
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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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A minimum 3 years experience beyond Sr Principal Scientist OR at least 10 years of drug discovery and development experience in the cardio metabolic space is required. Thanks to robust drug discovery/development and disease areas expertise, drives deep scientific evaluation of potentially transformational opportunities, working closely with functional partners, and provides scientific go-no-go recommendations for governance review.
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development discovery jobs in Blue Bell, PA
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