06 ago - Padova
Worldwide Clinical Trials
Worldwide Clinical Trials is seeking a Clinical Research Associate to monitor sites in registries and non-interventional studies. You will lead start-up activities, gather regulatory documents, and train site staff, while ensuring regulatory compliance and patient safety across trials.
The role emphasizes strong English communication, organization, and the ability to work with limited supervision, with most site work conducted remotely plus travel as needed.
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