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Act as main point of contact for the SVP, Heads of Drug Development for Immunology, CV and Neuroscience and Hematology and Oncology in thought leadership initiatives designed to elevate the company's scientific reputation in these therapeutic areas.
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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.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Key Responsibilities The Senior Principal Scientist will collaborate across BMS sites with Analytical, Drug Product, Drug Substance, Quality, and Regulatory leads to execute drug product formulation/process development support, analytical strategies for drug product methods and specifications, analytical control strategies, and support of product development up to drug application submissions and approval.
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A deep knowledge of neuroscience, therapeutic proteins and drug development across different biologics modalities. The Director of Biologics, Early Analytical Development is responsible for collaborating with DS (Drug substance), DPD (Drug product development), Drug delivery, Discovery and other cross-functional teams to support new and innovative toxin drug substance and drug delivery development.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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As a key member of their research and development team, you will leverage your expertise in computational chemistry and data analysis to support drug discovery efforts and advance their pipeline of therapeutic candidates.
Starting at $105,000 - $135,000 a yearFull-timeExpandUpdated 21 days ago - UpvoteDownvoteShare Job
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Key Responsibilities Provide medical leadership within Drug Safety Benefit-Risk Management Accountable for therapeutic area/product safety oversight and strategies/activities including (but not limited to): Strategic advisement on clinical development plans, design of clinical protocols.
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Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies, is recruiting for a Principal Scientist, Computer-Aided Drug Design (CADD, Computational Chemistry) located in San Diego, CA (La Jolla area.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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This will include formulation and commercial process development for biologics (monoclonal antibodies, antibody drug conjugates, bispecifics and fusion proteins). The Biologics Drug Product Development group develops monoclonal antibodies, antibody drug conjugates (ADC), and other biologics using state of the art formulation and process technologies.
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As a member of Gilead's patent prosecution team, you will work collaboratively on cross-functional research teams to advance research and clinical candidates through the drug development process.
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The team strives to deliver compelling preclinical, clinical, and translational data packages providing confidence in the dosing strategy, tolerability profile, and therapeutic efficacy of our candidate drugs to support investment in late-stage clinical development, leading to drug approval.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The successful candidate will have hematology/oncology clinical drug development experience, demonstrated leadership, and be able to critically navigate the science that underlies these programs.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Hematology Research and Development (R&D) team is accountable for all drug development activities in hematology research from first-in-man studies, all the way to late-stage trials leading to drug approval by regulatory agencies (Phase 1, 2, and 3 trials.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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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There will be also many valuable opportunities to participate in other projects that are crucial to the success of in vivo and ex vivo gene editing therapeutic drug development. Perform a variety of assays to support companywide analytical needs for the analysis of therapeutic biomolecules, e.g., adeno-associated virus (AAV), lipid nanoparticle (LNP), and/or cellular drug products.
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