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contact information for at least two referees who can supply letters of recommendation upon request. Inquiries and additional materials can be sent to lzahodne@umich.edu. Job Summary The Department
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | 5 days ago
compounding. Learning Objectives: Under the guidance of the mentor, you will gain skills and confidence in making scientific presentations; learn how to collect and compile clinical information; and learn
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: Conduct field and laboratory activities relating to evolutionary genetics including, but not limited to, sampling, collecting trait data, and extracting nucleic acids from samples. Conduct data analysis
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institution systems may be submitted. Click here for detailed information about acceptable transcripts. A current resume/CV, including academic history, employment history, relevant experiences, and
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internal institution systems may be submitted. Click here for detailed information about acceptable transcripts. A current resume/CV, including academic history, employment history, relevant experiences
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experience. Curriculum vitae (CV) including a list of publications. Contact information for three professional references. Applications should be sent via email to [CASTOR.Postings@umich.edu ] with the subject
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medicine, vascular biology, bioengineering, and data science, Dr. Chen leads an active research program focused on epigenetics, RNA and chromatin biology and endothelial stress response. Her team integrates
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Center for Drug Evaluation and Research (CDER) | Silver Spring, Maryland | United States | about 2 hours ago
: Conduct literature searches on specific monograph drug active ingredients using regulatory science databases and evaluate scientific evidence supporting safety and effectiveness determinations. Data
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are produced -- making the process cleaner, smarter, and more efficient. This is an opportunity to help reshape how critical materials are produced -- moving toward smarter, data-driven processes
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data collection and integration across multi-institutional collaborators. Work closely with clinical and research teams to ensure high-quality sample tracking, annotation, and compliance with