Clinical Research Associate
On-siteMilan, Lombardy, Italy
Milan, Lombardy, ItalyOn-siteFull TimeEntry LevelBachelors DegreeEnterprise
Full TimeEntry LevelBachelors DegreeEnterprise
Job Summary
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff to facilitate smooth study conduct, perform data review and query resolution, and contribute to the preparation and review of study documentation including protocols and clinical study reports. Requires approximately 60% travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a 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 a fast-paced environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.