CRA - FSP
KI-Beschreibung
In this role, you will be part of a dynamic team focused on delivering exceptional service across challenging projects. Your daily activities will involve coordinating clinical monitoring processes and engaging in continuous professional development.
Anforderungen
- •University degree in a life-sciences field
- •At least 6 months independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
- •Demonstrated understanding of ICH-GCP, EU and FDA requirements