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Stanford Securities Litigation Analytics is a research center within Stanford Law School focusing on public company shareholder litigation and corporate governance matters. SSLA closely collaborates with
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, and cellular and gene therapies. Research Project: CBER’s mission is to ensure the safety, purity, potency, and effectiveness of biological products including vaccines, blood and blood products, and
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | 10 days ago
database from randomized and controlled clinical trials for drugs intended to treat diabetes, overweight, and lipid disorders, enhancing FDA's safety signal detection capabilities. You will collaborate with
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 10 days ago
-the-counter and prescription drugs, including biological therapeutics and generic drugs. These efforts cover more than just medicines. Research Project: Pediatric developmental safety studies in drug
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research theme Work Futures and Economic Security. As a research-focused academic at Level A, you will work closely with senior researchers while progressively developing greater autonomy in your research
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 10 days ago
: This research project will examine the use of nonclinical in vitro studies to evaluate drug safety and support regulatory decision-making. Research involves using state-of-the-art automated patch clamp
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, specifically within the IRISA/Sotern teams, in cooperation with the LAB-STICC/Iris, all two experts research groups in network security. In collaboration with the project team and under the supervision
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | 10 days ago
, there are only animal data to inform the safety in pregnant and lactating women. Pregnancy safety and lactation data are collected predominantly in the post approval setting. The 2007 FDA Amendments Act gave FDA
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investigating harmful user-generated content in virtual worlds as part of a national research initiative on Online Trust and Safety. The primary responsibility of this role is to develop safety guidelines such as
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of a PhD degree. For more information see: http://www.mn.uio.no/english/research/phd/ All candidates and projects will have to undergo a check versus national export, sanctions and security regulations