AstraZeneca

The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, managing study supplies, and ensuring data quality through monitoring visits and source data review.

The Clinical Research Associate is locally responsible for study delivery at assigned sites, acting as the main contact for monitoring conduct to ensure compliance with guidelines like ICH-GCP and local regulations. Key duties include site preparation, initiation, monitoring, and closure, alongside training site staff and driving site performance.