Caitlyn Grubb

Caitlyn has worked with the MOR team in various aspects since joining the BPRU in 2018. Currently, she provides regulatory support in the form of FDA and IRB submissions, Clinical Trials updates, and staff training. Caitlyn also serves as a voting member on the Data Safety Monitoring Board. Caitlyn is currently working on her Masters in Drug Discovery and Development at Drexel College of Medicine and has an interest in novel therapeutics for pain, including their abuse liability, clinical development, and competitive landscape.

 In her free time, she likes to go adventuring with her fiancé and dog, binge watch NCIS, and bake delicious desserts.

 

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