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Role: A Project Manager at a Bioanalytical Contract Research Organisation (CRO) specializing in LC/MSMS bioanalytical services for drug discovery and development. Role: A Project Manager at a Bioanalytical Contract Research Organisation (CRO) specializing in LC/MSMS bioanalytical services for drug discovery and development.
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Overall description: This position in the Pharmacodynamics (PD) team offers a unique professional opportunity to gain in-depth exposure to industrial drug discovery and development from a proven research team.
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They are used in drug discovery, toxicity testing, stem cell banking, and cell therapy development. the development and documenting of new methods or equipment for cell processing unit operations including bioreactor-based cell culture, media manufacturing, cell washing and concentration.
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. The Center for Discovery and Innovation (CDI), was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases.
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The Research Associate / Senior Research Associate will primarily be responsible for the development and conduct of in vivo, ex vivo, as well as in vitro studies in Disease Biology and Translational Sciences to support the advancement of Septerna's small molecule drug discovery pipeline.
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Solid understanding of commercialization and the principles of drug discovery and development. Solid understanding of commercialization and the principles of drug discovery and development.
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The Machine Learning Engineer will work closely with the CTO to build the core data platform at the heart of the company’s drug discovery engine. You have previous experience in the application of machine learning to drug discovery.
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This position reports to the head of clinical pharmacology and toxicology and liaises with clinical development, clinical operations, non-clinical pharmacology and toxicology, and drug discovery to execute activities for advancing the development pipeline.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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Pharma: Counter ions, Leachables and Extractables, and Ionic Impurities in Drug Discovery, Development, Manufacturing. Oversee development of production plans and schedules that optimize plant manufacturing resources while at the same time provide the fastest, possible response to demands.
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Experience prosecuting drug discovery projects in a biotech or pharma environment, infectious diseases research is required; experience with drug development through initial clinical trials is advantageous.
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Serve as a leader supporting the overall CPP and/or translational medicine organizational objectives Stay current with scientific advancements and regulatory trends in clinical pharmacology and Pharmacometrics, and apply the knowledge to advance drug discovery and development for the organization; Publish in peer reviewed journals.
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Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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Inotiv is a growing contemporary drug discovery and development company where we Play to Win in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world.
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Candidate should be business orientated, having managed resources and budgets with proven record of leading projects trough successful transition from Discovery to Early Development and advancement of projects through preclinical and clinical development to Phase 2b within the therapeutic area.
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