Tonke van Bragt

Tonke van Bragt, partner of CURARE, has over 25 years of experience in pharmaceutical industry as a.o. Clinical Pharmacology lead, Project Lead and Regulatory Affairs Lead. She has been involved in many drug development programs in early and late stage development in various therapeutic areas including orphan diseases. She developed biologics as well as small molecules from research to Proof of Concept and to Market Authorization. Recent positions include Clinical Pharmacology Lead in a Global Pharmaceutical company and Project Lead and Clinical Pharmacology Lead in a BioTech Company.

Prior to co-founding CURARE, she was a senior consultant Clinical Development and Regulatory affairs at Kinesis Pharma, consultant Drug Development and Program Manager at the non-clinical contract research organization NOTOX B.V. (now Charles River), Clinical Pharmacology Research Manager and Regulatory Affairs Scientist at Organon (now Merck Sharp and Dohme) and Literature Scientist at the Dutch Poison and Control Center of the National Institute for Public Health and the Environment (RIVM).

She graduated in Medical Biology at the University of Utrecht, The Netherlands, in 1990 and holds a registration in Pharmaceutical Medicine (2011).