Clinical Research Associate II / Senior Clinical Research (CRA) - Italy

What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection Collect, review and track essential/regu…