Clinical Research Associate I — Site Monitoring & Trials

09 ago - Milano
Fortrea

Fortrea is seeking a Site Monitoring/CRA to oversee clinical study activities in Milan, ensuring adherence to SOPs and regulatory guidelines.
L'esperienza richiesta ai candidati, così come le competenze e le qualifiche aggiuntive necessarie per questo lavoro, sono elencate di seguito.
The role involves site visits, data integrity checks, and collaboration with vendors and internal teams.
The candidate must hold a Master's Degree in a scientific field, be CRA-certified, and be fluent in Italian and English.
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Willingness to travel and work in a matrix environment is required.
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