The Division of Applied Regulatory Science (DARS) in the Office of Clinical Pharmacology (OCP) and Office of Translational Science (OTS) in the Center for Drug Evaluation and Research (CDER) at the FDA has one opening for a safety informatics fellow to perform text mining research on FDA labels, MedWatch narratives, peer-reviewed literature, and regulatory documents. The fellow will also assist in developing models for predictive safety. He or she may additionally have the opportunity to learn about and work with pharmacogenomics and cheminformatics databases for incorporation into predictive models. Computational biology/chemistry/toxicology experience with the following programs is preferred: KNIME, R, Python and one or more text-mining programs.
Interested applicants should send a CV and a short narrative summarizing any relevant experience for the position. Forward to Yu.Lin at fda.hss.gov <mailto:Yu.Lin at fda.hss.gov> along with contact information and references.
Mentors for position:
Keith Burkhart, MD, FACMT
Senior Advisor for Medical Toxicology
Rebecca Racz, PharmD
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