Clinical Research Associate II
Excelya
- Αθήνα
- Μόνιμη
- Πλήρης Απασχόληση
- Ensure compliance with ICH-GCP guidelines, SOPs, and all applicable local and international legislation.
- Complete all sponsor-mandated trainings within set timelines and provide evidence of completion to internal teams.
- Conduct site monitoring visits to verify data accuracy, ensure protocol compliance, and support informed consent procedures.
- Facilitate communication between sponsor and site, acting as the primary link to ensure smooth clinical trial execution.
- Oversee regulatory submissions and track approvals from Ethics Committees and Regulatory Authorities to ensure study start-up timelines are met.
- Monitor and maintain drug accountability, ensuring proper shipment, storage, dispensing, and reconciliation across study sites.
- Experience: At least 2 years previous experience as CRA.
- Skills: Good communication and organization skills, focus to detail, time management, multi-tasking, very good knowledge of PC, willingness to travel.
- Education: Bachelor’s degree in life and/or health sciences is preferred - post graduate studies in a relative field are considered as a plus.
- Languages: Fluency in English and Greek language.