Clinical Research Associate II
KI-Beschreibung
In this role, you will manage multiple clinical study sites, ensuring compliance and accuracy in data collection. Daily activities will include site monitoring, report preparation, and collaboration with various teams to support clinical studies.
Anforderungen
1–4 Jahre- •18 months to 4 years of site monitoring experience in clinical research
- •Excellent understanding of GCP, ISO 14155, MDR, FDA, EU, and local clinical regulations
- •Fluent in Dutch and English; additional language skills are an asset