Senior CRA — Lead Global Trial Monitoring

3 ore fa

Bardi, Emilia-Romagna, Italia ICON Clinical Research Tempo pieno

ICON Plc is seeking a Senior Clinical Research Associate (CRA) to oversee monitoring activities in a sponsor-dedicated model.

Esperienza, qualifiche e soft skill: possiede tutti i requisiti per avere successo in questa opportunità? Lo scopra qui sotto.

You will ensure trials are conducted in compliance with protocol, GCP, and regulatory requirements, while fostering collaboration across functions.

You will lead site visits, assess performance, resolve issues, and train site staff to maintain high standards. xlwpduy

Travel up to 60% is required.