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The Earth Observatory of Singapore (EOS) is a Research Centre at Nanyang Technological University Singapore that conducts fundamental research on earthquakes, volcanic eruptions, tsunamis, and climate change in and around Southeast Asia, towards safer and more sustainable societies. EOS maintains...
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Center for Drug Evaluation and Research (CDER) | Jefferson, Arkansas | United States | about 2 months ago
- Automated Identification of Adverse Events from Drug Labeling Organization U.S. Food and Drug Administration (FDA) Reference Code FDA-CDER-2026-0136 How to Apply To submit your application, scroll to the
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characteristics of plants in annual and perennial cropping and native vegetation systems and their contribution as drivers of processes of soil carbon sequestration. The experimental component of the
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and briefing documents. Global Labeling Gain in-depth knowledge of labeling regulations regarding Company Core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC
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operationalize regulatory strategy. Support regulatory interactions with regulatory bodies including preparation of meeting requests and briefing documents. Global Labeling Gain in-depth knowledge of
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of drought on plant roots and their interactions with soil. The experimental component of the position will involve field soil and root sample collections from multiple experimental sites aimed at
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networks. Experience securing research funding, managing research programs, and building academic partnerships. Experience with embedded systems, FPGA/RTL, and RF technologies, and CUDA coding for GPU
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background in computer systems, GPU programming. Experience with CUDA, Triton, PyTorch, and LLM inference frameworks. Experience in research and good publication record. Track record first-author publications
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Labeling, for a period of 8 months each. The remaining 8 months of the program will be spent in a regulatory elective. Regulatory elective opportunities are offered in areas including CMC, Advertising
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-depth training in two distinct areas of GRA, Regulatory Strategy and Global Labeling, for a period of 8 months each. The remaining 8 months of the program will be spent in a regulatory elective