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and oligonucleotide therapeutics (ONTs), through the integration of nonclinical safety data evaluation and Model-Informed Drug Development (MIDD) approaches. Under the guidance of a mentor, you will
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spectrometry (GC-IRMS) capabilities. The project connects analytical chemistry theory with practice through method development, validation, documentation, quality systems, data interpretation, laboratory safety
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translation, technical assistance, training and partnership development. For more information, visit: https://www.cdc.gov/nccdphp/dcpc/index.htm https://www.cdc.gov/comprehensive-cancer-control/about/index.html
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scientific considerations that may influence generic drug quality, access, development pathways, and approval timelines across jurisdictions. You will engage in interdisciplinary research and training
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will be a part of data collection, analysis, modeling and simulation for this project. Learning Objectives: Under the guidance of a mentor, you will have the opportunity to learn about drug development
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pathology, bioinformatics, comparative evolution and other areas. You will also have opportunities to attend scientific conferences for presenting the research results and establish collaborative networks
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genomics, and pathogen discovery. The fellowship will focus on the development, evaluation, and application of advanced laboratory and sequencing approaches for the detection and characterization of known
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Office of Capacity Development and Applied Prevention Science (OCDAPS) in the planning, development, implementation, and evaluation of environmental medicine educational activities for clinicians. You will
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and analyze trait measurements related to plant development, plant physiology, and seed yield under different irrigation regimes in two locations with different weather patterns. You will also aid in
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ingredients (excipients) present in FDA-approved drug products, supporting both drug development and regulatory processes. This opportunity will provide you with hands-on exposure to the operational and