aCRM

The aCRM role is responsible for the end-to-end performance and project management of assigned clinical study protocols within a country, ensuring compliance with ICH/GCP guidelines and local regulations. This position serves as the primary liaison between Country Operations and the Clinical Trial Team, overseeing study execution, quality control, and risk management from feasibility through closeout. The role requires collaboration with local study teams, external partners, and global stakeholders to drive study success and maintain strong investigator relationships.