Clinical Research Associate (sponsor dedicated)
On-site · Warsaw, Mazovia, Poland
Job Summary
As a Clinical Research Associate II at ICON, you will design and analyse clinical trials, contributing to the advancement of innovative treatments. You will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials, ensure protocol compliance, data integrity, and patient safety, collaborate with investigators and site staff, perform data review and resolution of queries, and assist with the preparation and review of study documentation including protocols and clinical study reports.
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
- Willingness to travel approximately 60%
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