Clinical Research Associate, Site Management - Italy
IQVIA · Milan, Italy +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Compensation€33,900.00 - €61,700.00 base annually
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.