Clinical Research Associate
ICON · Milan, Italy
Clinical OperationsFull-timeCompany career page
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Role summary
A Clinical Research Associate II role focused on clinical trial monitoring in Milan. Responsibilities include site qualification, protocol compliance oversight, data integrity management, and investigator collaboration. The position requires a scientific degree, minimum 2 years CRA experience, knowledge of ICH-GCP guidelines, and willingness to travel approximately 60%.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate experience
- 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
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 resolve queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation including protocols and reports
Privacy & handoff
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