Description
The Lead Clinical Research Associate will lead a country- or regional-level clinical study team, oversee monitoring quality and compliance, coordinate with sites and cross-functional teams, manage monitors and study risks, support audits and CAPA, and mentor newly promoted Lead CRAs. The role emphasizes remote oversight with minimal to no site assignments and low travel, and requires at least four years of site monitoring experience, including participation in global clinical projects and experience monitoring sites in the United States.
