Sara has more then 10 years of experience in Life Science from pre-clinical and development phase to clinical phase. She started her career as a consultant within administration followed by quality, regulatory & compliance projects within the pharmaceutical companies such as Merck, GSK and Sanofi. She has also worked with project management in validation studies in the field of medical devices. As of 2018, she is a partner at Medicorent and works with outsourcing along with her own projects.
