Clinical Research Associate responsible for site monitoring and management across clinical trials in Italy. Ensures sites conduct studies in compliance with protocols, regulations, and sponsor requirements while managing recruitment, data quality, and documentation.
Responsibilities
Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
Develop and track subject recruitment plans with sites to meet enrollment targets
Evaluate study site practices for protocol adherence and regulatory compliance
Manage CRF completion, data queries, and maintain trial and investigator site files
Generate monitoring reports, follow-up correspondence, and other required documentation
Requirements
Master's degree in life sciences
CRA certification per Italian ministerial requirements
Completion of CRA training program or prior monitoring experience
Knowledge of GCP and ICH guidelines
Proficiency in Microsoft Office and laptop/mobile devices
Fluent written and verbal English communication
Strong organizational and problem-solving abilities
Compensation:
€33,****** - €61,****** base annually

📌 Clinical Research Associate, Site Management - Italy (Milano)
🏢 Iqvia
📍 Milano