Rebecca Lieberman

Rebecca Lieberman is a professional in regulatory affairs with extensive experience in clinical trial management. Currently serving as Manager of Regulatory Affairs at Deciphera Pharmaceuticals since April 2019, Rebecca has led global clinical trials and contributed to submission planning and strategic input for development programs. Previous roles include Senior Associate in Regulatory Operations & PM, overseeing US submission planning and Veeva RIMS implementation, and Senior Regulatory Coordinator at Dana-Farber Cancer Institute, where management of numerous industry-sponsored trials was a key responsibility. Earlier positions include Research Coordinator roles at LIFEPLANS INC and Beth Israel Deaconess Medical Center, where research project coordination and data management were central tasks. Rebecca holds a Bachelor of Science degree in Sociology from Boston University, graduating cum laude.