As the leader of Medidata’s Global Compliance & Strategy function,  Ari applies a risk based approach to navigating and interpreting the global regulatory landscape of the clinical trial ecosystem.  With nearly 25 years of experience working with regulated industries, Ari integrates cross functionally to bring a balanced application of compliance, governance, risk, and controls within Medidata’s products and services.  Leveraging the experience of an international team, Ari actively promotes increased trust and transparency regarding the areas that matter most in maximizing the potential of the Medidata Platform.

Dr. Ofra Levy-Hacham has served as our vice president of clinical and regulatory affairs since March 2018, and before that since joining us in 2011, she served as our vice president of quality and regulatory affairs. Prior to joining Sol-Gel, Dr. Levy-Hacham served as a scientific specialist and project manager at Biotechnology General Ltd., a fully integrated biopharmaceutical services private company from 2010 until 2011. From 2008 until 2010, Dr. Levy-Hacham served as vice president chemistry, manufacturing and controls at HealOr Ltd., a private company engaging in the development of therapeutics for the treatment of various skin lesions and conditions. Dr. Levy-Hacham holds a Ph.D. in chemistry from The Technion - Israel Institute of Technology, Israel.

Sharon Gai-Castro currently serves at Head of Clinical at Kamada, a commercial-stage global biopharmaceutical company with a portfolio of marketed products indicated for rare and serious conditions, and are a leader in the specialty plasma-derived field focused on diseases with limited treatment alternatives.

Prior to joining Kamada, Sharon held positions as Clinical Research Manager at Merck & Co. and Clinical Research Associate at Parexel.

Sharon holds a Master’s Degree in Neuroscience from Tel-Aviv University.

Ronen Mansuri currently serves as a Senior Biometrics Consultant, working for various Biotech companies in Israel including NeuroDerm, a clinical stage biotech company developing next-generation drug-device combination solutions for central nervous system disorders through proprietary drug formulations.

Prior to this Mr. Mansuri served as VP Clinical Operations & Biometrics at Galmed Pharmaceuticals and Senior Director, Head of Global Clinical Data Programming at Teva Pharmaceuticals. Ronen has vast experience in the Clinical Data Management and Statistical Programming areas for more than 20 years.

Mr. Ronen Mansuri is a PhD candidate in Personalized Medicine & Big Data Analytics in Tel Aviv University.

Ana is a Senior Solution Consultant at Medidata, specializing in Clinical Data Studio, working with clients on their clinical data management and study conduct strategies. Ana has a Masters in Neurobiology and 10 years of experience in SaaS technology, with the last 5 years focused on clinical trial technologies