Clinical Research Associate
ICON · Milan, Italy
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Research Associate role at a global healthcare intelligence and clinical research organization. The position involves designing and analyzing clinical trials, monitoring study sites, ensuring protocol compliance, and maintaining data integrity to support the development of new medicines and treatments.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 3 years experience as Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60% as required
- Legal right to work in Italy
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation including protocols and reports
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.