Senior CRA - FSP
KI-Beschreibung
In this role, you will engage in clinical monitoring across diverse projects, ensuring high-quality service while collaborating with international teams. Your daily responsibilities will involve taking ownership of your tasks and benefiting from extensive training to advance your expertise.
Anforderungen
5 Jahre- •At least 5 years independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
- •University degree in a life-sciences field
- •Demonstrated understanding of ICH-GCP, EU and FDA requirements