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