- 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,
📌 Clinical Research Associate (Level Dependent On Experience) (Torino)
🏢 Cti Clinical Trial And Consulting Services
📍 Torino
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