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Experience in oncology drug development. Extensive training and experience in the design and conduct of in vitro and in vivo preclinical pharmacology and toxicology studies directed at the development of pharmaceuticals or biologics.
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Cross-Functional Collaboration: Collaborate with internal stakeholders including medicinal chemistry, biology, toxicology, and clinical development teams to integrate DMPK data into drug development plans.
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Responsible for analytical development to support research and development, tech transfer and commercialization of drug substance and drug product processes, as well as oversight of batch testing/release and regulatory document contribution through managerial and individual input.
$182,250 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Knowledge of concepts related to drug discovery and development. PhD/MS in computer science, statistics, or computational science, with a focus on machine learning methods, or a PhD in a related field (e.g., computational chemistry or biology) with a strong emphasis in machine learning method development, and 10+ years of relevant experience.
$282,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Previous experience with genetic medicine, viral vectors, gene therapy, AAV, gene editing drug development/toxicology/regulatory interactions or ocular toxicology/drug development/regulatory toxicology experience is strongly preferred.
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Process Development Scientist (Formulation & Drug Product Development) In this vital role you will support Formulation & Drug Product Development at Amgen's site in Rockville, MD. This group is responsible for drug product formulation and process development for biologics in Amgens Rare Disease Business Unit. Working closely with a team of scientists and engineers, the successful candidate will apply scientific and engineering principles to advance the technical aspects of Amgens drug product and process development.
$129,162 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Executive Director Analytical Sciences & Technology will lead the analytical development encompassing method development, qualification, and cell therapy drug substances and drug product characterization for all cell therapy programs during product lifecycle.
$328,900 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Drive cross-functional collaboration across our data science, machine learning, lab informatics, and medicinal chemistry teams to advance our computational infrastructure for our drug discovery and development mission.
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This position offers a unique opportunity to work in a dynamic and innovative environment developing your career at the interface of mechanistic research, drug discovery, and preclinical drug development.
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We are seeking a Director, Pharmacovigilance and Drug Safety (Operations & Compliance) to join our team. Provides oversight of case processing activities for the Xenon clinical development program and serves as safety data management subject matter expert (SME) on regulations and best practices for conventions and handling of safety data in Xenon’s global safety database (GSDB.
$239,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Regulatory, CMC, drug development, pharmaceutical, biotech, chemical engineering, GMP, IND, IMPD/CTA, NDA, MAA. 10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs and small molecules.
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Hazardous Drug Delivery Sales Specialist. B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry.
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You have strong expertise in immuno-oncology and will be focused on focus on the development of fit-for-purpose CMC assays using flow cytometry and cell-based immunoassays, to characterize engineered TCR-T cell drug substance and drug product.
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Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
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ResponsibilitiesAssist in the creation, development and preparation of CDISC ADaM/SDTM data sets (ADPC, PP and ADPP) and data for global organization’s state-of-the-art medicinal and pharmaceutical analysis, such as PopPK or drug exposure-response (Pharmacokinetics/ Pharmacodynamics or PKPD), using company’s bio-simulation software, technology and tools/services in order to transform traditional drug discovery and development.
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drug development jobs Title: senior accountant Company: Charles River Laboratories
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