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scientists and software engineers. The team focuses on the following LISA deliverables agreed upon with the Norwegian Space Agency and ESA: Deliverable 1: Deployment and development of Norway’s computational
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. The post will contribute to the development and evaluation of trustworthy AI approaches that support high-quality clinical documentation and safer decision-making in dental care. You will help deliver co
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of SGLT2 inhibitors using mice models of kidney diseases. Contributing to the development of uremic toxin measurements in mice and human. Collaborating with faculty and staff on research design, data
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interactions in response to salinity stress. Collaborate on biofertilizer development incorporating beneficial microbial enzymes. Required Qualifications: Ph.D. in Microbiology, Bioinformatics, Soil Science
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for Empowerment, which focuses on identifying learning and competence development needs among students, teachers, school leaders, and other educational stakeholders. The cluster emphasizes AI literacy, professional
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believes in continuous learning and development Proficient in technical writing and presentation Possess strong analytical and critical thinking skills Show strong initiative and take ownership of work
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 6 hours ago
of pregnancy and lactation postmarketing requirement studies. Pregnant and lactating women have historically been excluded from drug development trials. Therefore, at the time of new drug/biologic approval
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 6 hours ago
unstructured submission data for model development; 2) Apply AI methods to identify key clinical and biomarker features that drive response to therapy; 3) Contribute to manuscripts, reports, and presentations
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for, disentangling selection and causal effects for the proposed research questions. The proposal must include a paragraph declaring if and how AI was used in the development of the proposal. Applicants should have
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will research topics related to the regulation of human drug compounding, including, but not limited to specific bulk drug substances that are used in compounding, advancing FDA's development of the Bulk