Travel-Ready Clinical Site Monitor (CRA)

Merck is seeking a Clinical Research Associate (CRA) to manage clinical trial sites across assigned protocols and sites in the United States. The role emphasizes building and maintaining site relationships, monitoring visits, and ensuring adherence to ICH-GCP, regulatory requirements, and study SOPs. The candidate will travel domestically and internationally, with a significant travel footprint of approximately 65–75% of working time, and will manage regulatory documentation throughout start-up, #J-18808-Ljbffr Merck