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Dr. Nadya Lisovoder 



Nadya is an accomplished doctor of medicine with over fifteen years of domestic and international experience in academic and clinical studies in the pharmaceutical, diagnostic, and medical devices industry. She is a regulatory expert and has been a clinical adviser to public biotech companies and a range of incubator and accelerator programs, including FutuRx—a Johnson & Johnson Innovation and Takeda Pharmaceutical Company program.

Nadya has managed clinical trials across multiple therapy areas in complex multisite studies across Israel, Europe, and the US for large pharma companies, such as Schering-Plough, as well as innovative start-ups. Since 2012, she has been leading the Israeli government’s biomedical research in seven hospitals in northern Israel, alongside universities, international pharma companies, global contract research organizations, and biotech companies.

Prof. Itamar Shalit

Senior Consultant


​Itamar earned his MD at the Sackler Faculty of Medicine at Tel Aviv University. He completed his fellowship in pediatric infectious diseases at the Children's Memorial Hospital in Oklahoma City and earned a master’s degree in public administration from the Kennedy School of Government at Harvard University.

Rivki Sten-Youdkevich

Senior Business Advisor


Rivki is a seasoned entrepreneur, having built and sold various social and ecological ventures, and is
an active investor in the field of cannabis. She is a certified public accountant and holds a master’s
degree in international management with 23 years of global entrepreneurial, financial, and business
development experience, which she gained as a consultant and executive.

Regulation team

The team is accountable for
regulatory submissions to various
ethics committees and ministries of
health worldwide.

Monitoring team

The monitoring team is responsible
for overseeing trials, recruitments of
patients, and any queries. They manage
and monitor each test, to ensure they
are following protocol and regulatory

Bio-statistics experts

Senior professionals, responsible for trial planning and statistical analysis. Highly experienced with FDA & EMA projects,

Scientific writing

Galilee CBR has a highly trained writer that is skilled in working with the FDA and EMA.

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