Overview As a Clinical Research Associate at Alira Health, you will lead site monitoring for clinical trials with independence and collaboration. You’ll work with in-house CRAs, Lead CRAs, and project managers to ensure protocol compliance, address site questions, and support study recruitment and training. You will drive data integrity through source reviews, AE reporting, and regulatory document reviews, while maintaining strong site relationships. This role offers hands‑on impact across monitoring activities, data quality, and site operations within a global, values‑driven culture. You will thrive in a fast‑paced environment, traveling as needed to ensure GCP compliance and study progress.Prepare monitoring visit reports detailing site issues,



resolutions, protocol deviations, and enrollment status
Facilitate adverse event reporting and reconcile SAE reports with source data and CRFs
Ensure CRF data integrity via source document verification
Conduct investigational product accountability and regulatory binder reviews
Collaborate with in‑house CRAs and data management to resolve data discrepancies
Maintain regular site contact to ensure protocol/GCP compliance and monitor patient accrual
2 years of clinical research experience

📌 Research Associate (Italia)
🏢 Experteer Italy
📍 Italia