Experienced CRA, Sponsor Dedicated - Italy
IQVIA · Milan, Italy +1 more
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate needed to perform site monitoring and management for clinical trials in Italy. Responsible for conducting monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation in accordance with GCP guidelines.
What they're looking for
- Bachelor's and Master's degree in scientific or healthcare discipline
- Minimum 3 years of on-site clinical monitoring experience
- CRA certification per Italian Ministerial Decree 15.11.2011
- Strong knowledge of GCP and ICH guidelines
- Proficiency in Microsoft Office and standard computer systems
- Fluent English, written and verbal communication skills
- Organizational and problem-solving abilities
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and closeout
- Develop and track subject recruitment plans with assigned sites
- Administer protocol training and maintain regular communication with sites
- Evaluate site compliance with protocol and regulatory requirements
- Track study progress including regulatory submissions, enrollment, and data queries
Compensation€33,900–€66,700 base annual salary
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.