Lisa Sherman is Vice President of Clinical Operations with over 22 years of experience in clinical research across the biotechnology and pharmaceutical industries. She holds a Bachelor’s degree in Kinesiology and a Master’s degree in Business Administration Healthcare Management. She began her career at The University of Texas MD Anderson Cancer Center in the Office of Protocol Research. Throughout her career, Lisa has held leadership roles spanning academia, regulatory affairs, clinical operations, and project management. She has successfully supported multiple NDA, BLA, and MAA submissions and has led organizations through FDA, Health Canada, MHRA, and EMA regulatory inspections with no major findings. Lisa brings extensive experience overseeing multiple clinical programs simultaneously, managing multimillion-dollar budgets, and driving operational excellence to advance complex development portfolios.
