临床监查员【校园招聘】

Position Summary
Responsible for the site monitoring an******** of all aspects ofclinical studies assigne******** accordance with ICH-GCP, an********regulatory re******** an******** Standar******** Procedures (SOPs) ofSponsor and /or dMed. CRA needs to be flexible to manage variousprojects an******** to handle different therapeutic areas an********studies. Buil******** maintain the working relationship with sitean********. The degree (CRA I & II & an********. CRA) ofresponsibility accorde******** a CRA will reflect their level ofexperience an******** that they can make to the project.

Education an******** Competency Requirements
- Medical or pharmaceutical education backgroun******** other lifescience degrees (or equivalent); clinic practice is preferred
- Goo******** knowledge of GCP guidelines
- Proficiency in Basic Microsoft Wor******** Excel an******** with useof database
- Knowledge of drug development process