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For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
$114,375 - $190,625 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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For more than 20 years, its passionate, innovative and collaborative team has invented next- antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next- immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
$170,625 - $284,375 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Operational and technical expertise on LC-MS, GC-MS and ICP-MS instrumentation Thorough knowledge on Extractable and Leachable testing and elemental impurity testing Strong interpretation skills and technical expertise in impurity identification in the drug products and drug substances Ability to establish and maintain working relationships with co-workers.
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It offers services in the areas of custom synthesis/contract research, process and analytical research, cGMP synthesis, crystallization process development, solid form screening and selection, pre/early formulation, and drug substance-drug product coprocessing.
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Chemistry is a core capability in Small Molecule & Drug Discovery with innovative scientists working in medicinal chemistry, radiochemistry, analytical chemistry, and large-scale synthesis. Bristol Myers Squibb encompasses a broad range of disciplines to enable a robust pipeline of drug candidates aimed at serious diseases.
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Genmab is now searching for an experienced Senior IRT/Systems Manager to be part of Global Clinical Drug Supply, CMC Operations, and work according to our hybrid work arrangement in Princeton, NJ.
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Safe and timely execution of Phase I studies; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations.
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A Japan-based company, our goal is to make people smile by delivering breakthroughs where no adequate treatments currently exist, working from drug discovery to product development and commercialization.
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Provide strategic CMC regulatory expertise for development project teamsProvide strategic input to development & GO teams to mitigate drug supply issues. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
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Reporting to the Head of US and Above Market Compliance and Ethics Organization, this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and integrate one global compliance program into the US and Worldwide Commercialization Organizations.
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Implement and drive innovative drug discovery strategies utilizing deep expertise across medicinal chemistry and synthetic chemistry route design, through comprehensive knowledge of DMPK, pharmacology, and toxicology.
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Incumbents with a Master's degree in counseling or social work not possessing any of the qualifications specified in (a) above shall obtain LCADC status by December 1, 2022, or another health professional license that includes diagnostic and supervisory authority for work of an alcohol and drug counseling nature.
$100,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Significant experience in pharmaceutical/biotechnology and extensive knowledge of drug development processes, ICH-GCP guidelines, 21 CRF Part 11, and major Health Authority regulations as they pertain to the operational aspects of clinical trials.
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Serve as a contact for all TK-related issues pertinent to the development of assigned drug candidates and closely interact with study directors, project representatives, bioanalytical scientists, and other relevant functional areas.
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Enhance technical documents by creating simple graphs, charts, screen-captures, block/flowchart diagrams, and images using software like MS PowerPoint, MS Visio, and Techsmith Snag-It. Enhance technical documents by creating simple graphs, charts, screen-captures, block/flowchart diagrams, and images using software like MS PowerPoint, MS Visio, and Techsmith Snag-It.
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drug screen jobs Title: diesel technician Company: Energy Jobline in Monmouth Junction, NJ
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