If you have a Life Science clinical question, bring it to Stephanie Lustgarten. She has nearly 15 years of experience in clinical development in the life sciences/biotechnology/pharmaceutical industry with a focus in oncology. Additionally, she has experience in phase I through phase III clinical trials and has lead global regulatory submissions from a clinical data sciences perspective, including New Drug Applications (NDA) and Marketing Authorization Application (MAA).
Stephanie received her PhD in biostatistics from Boston University and has worked at small, mid-size and larger life sciences organizations within the Boston area.
