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ingredients, sophisticated formulations, and innovative dosage forms; Advance Human Subject Safety for Bioequivalence Studies - Conducting meta-analysis to determine appropriate safety strategies to ensure
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: You will develop skills in safety signal detection, learn to identify data quality issues that could obscure safety signals, and understand challenges in identifying rare adverse events in minority
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The Japan Society for the Promotion of Science (JSPS) has established the JSPS Postdoctoral Fellowships for Research in Japan – Standard program. A limited number of promising early career
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rigorous research, the practical applications of code exfiltration and reverse engineering as well as security penetration testing. The primary responsibility of this role is to deliver on an industry
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Center for Drug Evaluation and Research (CDER) | Jefferson, Arkansas | United States | about 22 hours ago
join generations of scientists in the field of pharmacoepidemiology, pharmacovigilance, and drug safety through this learning opportunity. You will receive mentorship by experts in the field, which is a
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Center for Devices and Radiological Health (CDRH) | Southern Md Facility, Maryland | United States | about 21 hours ago
. Research Project: The FDA's CDRH Ophthalmic Device Program ensures safe and effective innovative ophthalmology devices including diagnostic retinal imagers and therapeutic devices like prostheses, lasers
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battery data. Develop scalable, secure, and production-grade software systems supporting industrial deployments. Integrate embedded BMS firmware, edge computing devices, and cloud analytics pipelines
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will publish relevant results to cryptography conferences/journals Job Requirements: PhD in Mathematics and/or Electronics and/or Computer Science Ability to work independently and as part of a team with
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Center for Drug Evaluation and Research (CDER) | Jefferson, Arkansas | United States | about 22 hours ago
for causality assessments of individual case safety reports. The research project is supported under 21st Century Cures Act (2016) Section 3022 (Drug Safety) to evaluate real-world evidence data on drug’s use
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 6 days ago
research questions involving challenging active/inactive ingredients, sophisticated formulations, and innovative dosage forms; 3) Advanced human subject safety for bioequivalence trials - Conduct meta