Description
The Lead Clinical Research Associate will lead a clinical study team at a country or regional level, overseeing monitoring quality, compliance, data integrity, study risks, investigator-product and supply management, audits, CAPA, safety reporting, and project-team coordination. The role emphasizes remote oversight and mentorship rather than direct site management, with minimal to no site assignments and a low-travel model. Candidates need relevant life-science education, at least four years of site-monitoring experience on global clinical projects, United States site-monitoring experience, and experience with Phase II or III monitoring visits; oncology, cell therapy, gene therapy, nuclear medicine, and gastrointestinal disease experience are preferred.
