Clinical Research Associate Sponsor-dedicated
IQVIA · Athens, Greece
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a Clinical Research Associate to perform site monitoring and management activities for clinical studies in Greece. The role ensures sites conduct studies according to protocol, regulations, and sponsor requirements while managing recruitment, data quality, and regulatory compliance.
What they're looking for
- High school diploma or degree in scientific or healthcare field preferred
- Minimum 1 year of on-site clinical monitoring experience
- Strong knowledge of GCP and ICH guidelines
- Proficiency in Microsoft Word, Excel, PowerPoint and standard computer systems
- Fluent written and verbal communication in Greek and English
- Organizational, problem-solving, and time management skills
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
- Collaborate with sites on subject recruitment planning and track enrollment progress
- Administer protocol training and maintain regular communication with assigned sites
- Evaluate site compliance with protocol and regulatory requirements; escalate quality issues
- Maintain study documentation including trial master files and investigator site files
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.