Senior Clinical Research Associate
KI-Beschreibung
In this role, you will oversee clinical trial activities, ensuring compliance with protocols and regulations. Daily tasks will involve monitoring sites, conducting visits, and collaborating with teams to maintain data integrity and participant safety.
Anforderungen
ca. 4 – 6 Jahre- •Extensive experience as a Clinical Research Associate
- •Strong understanding of clinical trial processes and regulatory requirements
- •Proficiency in relevant clinical trial software and tools