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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 18 hours ago
therapeutics and generic drugs. These efforts cover more than just medicines. Research Project: Safety assessments for medications intended to treat psychiatric conditions present unique challenges in signal
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 17 hours ago
turn this project will advance safety and understanding of potential toxicity of FDA-regulated products in the perinatal population. Learning Objectives: Under the guidance of the mentor, you will gain
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 18 hours 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 | about 17 hours 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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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 18 hours 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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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 18 hours 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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Future of Life Institute: Vitalik Buterin Postdoctoral Fellowship in AI Existential Safety Eligibility: To be eligible, applicants should identify a mentor (typically a professor) at the host
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this cross-functional role, the postdoctoral fellow will develop AI-driven methodologies to bridge the gap between genomic evidence and safety outcomes, addressing a critical challenge in pharmaceutical
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are reviewed regularly and are subject to change. To apply, visit https://northeastern.wd1.myworkdayjobs.com/en-US/careers/job/Boston-MA-Main-Campus/Alnylam-Pharmaceuticals-Global-Patient-Safety-and-Risk
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, and scholarly activities. In partnership with Northeastern University, Alnylam Pharmaceuticals is offering a two-year Global Patient Safety and Risk Management fellowship, based in Cambridge, MA. About