About Us

Dr. Lisa Levine is a distinguished clinical trials leader with a career dedicated to generating high-quality clinical evidence to support market authorization, adoption, and reimbursement of medical devices. Passionate about enhancing global healthcare, Dr. Levine has thirty years of international involvement in clinical evidence development and distribution strategies.

Experienced in first-in-human studies, feasibility and pivotal studies, post-market studies, registries, and investigator-initiated studies. Dr. Levine’s expertise involves permanent implants, software, and hardware medical devices.

Dr. Levine earned her undergraduate degree in Physics from the California Institute of Technology and her PhD in Biophysics from Stanford University. She has held significant leadership roles throughout her career, including Vice President of Clinical and Pre-Market Regulatory Affairs at Calypso Medical, where she led efforts to develop products and software for real-time tumor tracking and motion management during radiosurgery and radiotherapy. At Varian, she held the position of Senior Director of Clinical Operations, overseeing investigator-initiated studies and multinational trials across the US, Canada, UK, Germany, Switzerland, Denmark, Netherlands, Italy, Belgium, Australia, China, and South Africa.