Clinical Research Associate
Excelya
- Αθήνα
- Μόνιμη
- Πλήρης Απασχόληση
- Deeply acknowledges and strictly follows SOPs, ICH-GCP guidelines and appropriate local and international legislation.
- Acts as the main link between sponsor and the investigator.
- Must be in the position to fully explain the purposes, the set-up and the procedures of the clinical trial to the investigators, train site staff as needed and assist them in the conduct of clinical trials.
- Is responsible for adequate monitoring of the clinical trial conduct at the investigational sites.
- In case of an audit or regulatory inspection, is responsible for informing and preparing the site and facilitating the procedure. In collaboration with the appropriate Managers supervise that the corrective actions are performed as soon as possible.
- Ensures compliance with applicable quality standards, i.e. SOPs, ICH-GCP and legislation.
- Experience: At least 1 year of 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.