CTI Clinical Trial and Consulting Services in Italy seeks a Clinical Research Associate to serve as main CTI contact for assigned study sites and to conduct monitoring visits in line with ICH-GCP. You will support start-up activities, manage essential regulatory documents, participate in team meetings, and help ensure accurate IP storage and trial materials.
Fluent English is required; a life science background is preferred.
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📌 Clinical Research Associate – Site Monitoring & Start-Up (Roma)
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📍 Roma
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