Experienced Clinical Research Associate Sponsor-dedicated
IQVIA · Athens, Greece
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
The Clinical Research Associate Sponsor-dedicated role involves conducting site monitoring visits, managing study progress, and ensuring protocol compliance across assigned clinical trials. Candidates need at least 2 years of on-site monitoring experience, strong knowledge of GCP and ICH guidelines, and fluency in Greek and English.
What they're looking for
- Minimum 2 years on-site clinical trial monitoring experience
- High school diploma or equivalent; scientific or healthcare degree preferred
- Knowledge of GCP and ICH guidelines for clinical research
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Fluent written and verbal communication in Greek and English
- Strong organizational and problem-solving capabilities
- Ability to build effective working relationships with diverse stakeholders
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
- Deliver protocol training to assigned sites and maintain regular communication
- Evaluate site compliance with protocol, regulations, and GCP standards
- Manage study progress by tracking regulatory submissions, enrollment, CRF completion, and data queries
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.