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The Biologics group is responsible for various functions criticalfor drug development such as: antibody discovery, molecular biology, cell line engineering,protein engineering, biophysical analytics, and functional cell assays.
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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.
$150,000 - $170,000 a yearFull-timeExpandUpdated 14 days ago - UpvoteDownvoteShare Job
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This role is primarily focused on CMO(s) for AAV/gene therapy drug substance manufacturing. Manage and oversee cGMP operations at Adverum's drug substance CMO to ensure manufacture of Adverum products on-time and meeting quality, compliance, and applicable regulatory requirements.
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Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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Learning Agility - This role will require the ability to quickly build strong technical knowledge of the Guardant Health products and services for the Biopharma audience, in addition to understanding the BioPharma customer needs across precision oncology drug development.
$104,400 - $187,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Leads teams through drug development and manufacturing with an ability to understand and anticipate cross-functional challenges. He/she will serve as a key link between the drug product MSAT function and other functional groups across the Technical Development organization at Gilead, to ensure seamless partnership and progress on organizational objectives.
$237,660 - $307,560Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This position supports the company's Discovery Research function to advance preclinical drug development scientific initiatives. Demonstrates strong analytical skills requiring the application of scientific theory and creative skills in the development of hypotheses and experimental approaches.
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Performs analytical testing, method development, and bioanalytical characterization of innovative biotherapeutic proteins, including antibodies, bispecific proteins, and antibody drug conjugates.
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The Formulation & Process Development group located at the Foster City, CA Gilead headquarters is seeking a Senior Research Scientist I to provide scientific, technical and hands-on support of drug discovery and product development related to small molecules.
$177,905 - $230,230 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a minimum, Ph. D. in Toxicology, Pharmacology, Pathology, Biochemistry or Biology with extensive pharmaceutical industry experience in drug development toxicology. Experience in Discovery Toxicology as applicable to early stages (non IND-enabling) drug development would be a plus.
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Your responsibilities will include working closely with our drug development team (Senior Scientist, In vivo scientist, CEO, CSO, Chemists, and Toxicologists) to understand the efficacy of our small molecules discovered through our novel platform.
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Reporting to the Head of Molecular Biology, this position will also enable mechanism-of-action studies of MapLight drug targets which will provide foundational support for progressing new therapies into clinical development.
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The primary responsibility of a Research Scientist in a Pharmacokinetics Analyst role is to add to and enhance the ability of the drug metabolism and pharmacokinetics department to support discovery and development project teams.
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Seeks professional development by monitoring ones performance, solicits for constructive feedback, and leverages healthcare supervisor and store manager as mentor and coach. Leads efforts on enhancing patient experience by increasing awareness of healthcare services offered through Walgreens (e.g. patient consultation, medication management, drug therapy reviews, and perform clinical, or wellness services such as immunizations, diagnostic testing, and patient outcomes services) thereby promoting the shift of the Walgreens pharmacy role from transactional to interpersonal.
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drug development jobs in Palo Alto, CA
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