Anne-Lise Perrier joined MC Toxicology Consulting in 2015 as a consultant and project manager. She has more than 15 years of experience in non-clinical R&D mostly gained in the CRO sector. Most recently, she has worked at Aurigon Life Science, a German full service non-clinical CRO, as a study director in pharmacology, safety pharmacology and regulatory toxicology. As a project manager for non-clinical programs, she has been involved in the development of numerous drug candidates (small molecules, biologics, biosimilars, ATMPs, herbals and vaccines), many of which have been successfully marketed in Europe, the USA and Canada. Prior to Aurigon Life Science, she was an associate scientist at IDEA AG (Munich, Germany). Anne-Lise is a biologist and graduated from the Pharmaceutical University in Paris (France) with a Master’s degree in Drug Metabolism and Pharmacokinetics. She is currently attending the postgraduate Project Management Professional (PMP®) certification program.

 Toxicology, Pharmacology, and Pharmacokinetics