Clinical Research Associate
ICON · Milan, Italy
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate II position at a large contract research organization focused on sponsor-dedicated clinical trial monitoring. The role involves site management, protocol compliance oversight, and data quality assurance across multiple therapeutic studies.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulations
- Strong organizational and communication skills with meticulous attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60% as required
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff to support study execution
- Review clinical data and resolve data queries to maintain quality standards
- Prepare and review study documentation including protocols and clinical reports
Compensation€40,944.00-€51,180.00
Privacy & handoff
This role links to ICON'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.