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Communicate with cross functional teams as DMPK project representative to advance projects through the drug development process. A track record of driving DMPK projects with a focus on drug disposition.
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This influential and self-sufficient position will make significant contributions to drug discovery, preclinical studies, biomarker identification and development, and nonclinical research.
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The Metropolitan Council's Occupational Health Department (A unit within Human Resources) has one (1) vacancy for a full-time DOT Drug and Alcohol Program Compliance Coordinator. Human Resourcesworks with all divisions of the Metropolitan Council to provide proactive solutions for the Council's workforce needs in the areas of recruitment, hiring, labor relations, benefits, training, organizational development, occupational health, and wellness.
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A strong background in business development and/or account management within specialty chemical sales into the pharmaceutical drug development and drug manufacturing sector.
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Reporting into the Business Director - Pharma, North America, this is a newly created role and an opportunity for an individual, passionate about all aspects of drug delivery, including lipid nanoparticles and nucleic acid delivery to join a regional sales team and support business growth in one of our key strategic markets.
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Prospect and drive business development activities to scope out new opportunities for Croda’s excipients, adjuvants and lipids into Small Molecule, Protein Delivery, Nucleic Acid Delivery and Vaccine applications with a focus on double digit organic growth.
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The Drug Authorization Specialist, with direct supervision of the Prior Authorization Supervisor, is responsible for managing all work related to drug authorizations for all injectable drug treatment plans ordered by Dana Farber Cancer Institute providers using knowledge of payer coverage policies and applies appropriate payer guidelines to all aspects of drug prior authorization work.
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This position will be responsible for developing and executing robust epidemiology plans for Genmab product portfolio and pipeline in alignment with clinical development, global drug safety and pharmacovigilance and commercialization strategy.
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Provide analytical data to support drug substance and drug product development, including purity analysis, chiral purity and structure elucidation using mass spectrometry. 2+ year’s post-PhD experience in the pharmaceutical or biotech industry, focusing on process and product development, and analytical method development for drug substances and products.
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Our integrated service offerings include antibody discovery, recombinant protein production and purification, stable cell line development, protein analytics, comprehensive process development and non GMP/cGMP manufacturing.
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3+ years’ experience in the pharmaceutical or biotech industry, focusing on process and product development, and analytical method development for peptide drug substances and products.
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P fizer's Pharmacokinetics Dynamics and Metabolism (PDM) group in Andover MA is responsible for development and implementation of a variety of bioanalytical assays supporting drug discovery and development program.
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Solid understanding of the principles of ADME/Tox in drug discovery and development. Experience with real-world evidence for drug development projects. At Atomwise, we pioneered deep learning neural network approaches for structure-based small molecule drug discovery.
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As a Senior Scientist, you will work within the RNA Medicine team to develop a novel nucleic acid drug development platform. Innovate: Lead multiple drug discovery and development projects.
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Louisiana Cat is a drug-free workplace, including marijuana and THC products. Louisiana Cat (Louisiana Machinery Co, LLC) and its affiliates are drug-free workplaces and post-offer, pre-employment process includes background check, drug/alcohol screen, and if applicable for the role, pre-employment physical/fit for duty assessments.
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drug development jobs Company: Genoskin
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