Matteo Mosso

Matteo Mosso is Director, Clinical Affairs at Donawa Lifescience where he has managed and monitored international medical device and in vitro diagnostic (IVD) clinical studies since 2013. Matteo has over 20 years’ experience in the conduct and management of clinical studies. He began his career at Merck Sharp & Dohme (MSD), first as a Clinical Research Associate and then as Project Manager, gaining wide experience in several therapeutic areas, including Cardiovascular, Endocrinology, Oncology, Neurology and Psychiatry. During this time, he managed and coordinated study teams from start-up to close-out, together with site pre-study inspections, on-site audits, and site follow-up activities. Matteo subsequently worked at Covance, where he became Clinical Operations / Compliance Oversight Lead on assignment with Pfizer. In this new role he was responsible for in-country project management, oversight, and coordination of international CROs, oversight responsibilities for study monitoring, workload prioritization, study issue resolution, and coordination with corporate, medical, and clinical research staff and key opinion leaders. He holds a degree in chemistry from University of Rome ‘La Sapienza.’