Associate Director, Clinical Quality Assurance

Independently conduct Clinical Investigator Site Audits, Vendor Audits, GCP Document Audits (Clinical Study Reports and Trial Master Files), internal Process Audits and support System audits. The Associate Director, GCP Quality Assurance works within the Global Clinical Quality team to conduct GCP compliance activities at Eisai, at our CROs and Investigator Sites, and leading GCP audits and inspection readiness.