Rosanne Petros, PMPAssociate Director, Clinical Research at Merck Research Laboratories
Rosanne has 32 years of experience in clinical research, beginning her career as a CRA with a CRO in 1988. She continued her career in primarily project management at a CRO, as an independent consultant and for the last 15 years at Schering Plough/Merck. For the past 10 years, Rosanne has been involved in risk based operational oversight and risk-based monitoring. She routinely is invited to speak at industry conferences including last summer’s FDA public workshop on RBM. Rosanne has been involved in the selection and piloting of RBM systems within Merck. She was the lead author on an article published in February 2019 in the Journal of Clinical Research Best Practices comparing two different clinical research risk identification tools. She lives in the suburbs of DC in Maryland with her husband, 5 children and 2 dogs.