Clinical Research Associate 2 - IQVIA Biotech
IQVIA · Madrid, Spain +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA Biotech seeks a Clinical Research Associate to conduct site monitoring across multiple therapeutic areas in Spain. The role involves managing clinical trial sites, ensuring regulatory compliance, tracking enrollment and data quality, and collaborating with study teams throughout clinical development.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- Minimum 1.5 years of on-site clinical monitoring experience
- Strong organizational, time management, and problem-solving abilities
- Ability to build effective working relationships with sites and internal teams
- Willingness to travel across assigned sites
- Valid driver's license
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits per GCP and ICH guidelines
- Develop and track subject recruitment plans with sites to meet enrollment targets
- Provide protocol training and maintain ongoing communication with study sites
- Monitor study progress including regulatory approvals, enrollment, CRF completion, and data queries
- Maintain trial documentation in Trial Master File and Investigator's Site File per regulatory standards
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.