06 ago - Uri
Altro
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.
Legga la panoramica di questa opportunità per capire quali competenze sono richieste, incluse le soft skill pertinenti e la padronanza di pacchetti software.
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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Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.
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