Clinical Research Associate
On-site · Athens, Attica, Greece
Job Summary
Clinical Research Associate II responsible for designing and analyzing clinical trials, conducting site qualification/initiation/monitoring/close-out visits, ensuring protocol compliance and data integrity, safeguarding patient safety, collaborating with investigators and site staff, performing data review and resolving queries, and contributing to preparation/review of study documentation including protocols and clinical study reports. Requires a Bachelor's in a scientific/healthcare field, at least 2 years of CRA experience, thorough knowledge of clinical trial processes and ICH-GCP, strong organizational/communication skills, ability to work independently and with others, and willingness to travel (~60%). Employment with ICON contingent on legal right to work in the country of role; remote/hybrid options not specified beyond travel expectations.
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
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