Clinical Research Associate II-Guangzhou
ICON
- 广东省广州市
- 长期
- 全职
Shenyang office basedResponsibilitiesWhat you will be doing:
- Site Monitoring
- Site Management
- Ultimately reponsible for the successful management of investigator sites throughout the site lifecycle
- Working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard operating Procedures
- Bachelor degree or above
- Has more than 2 year of oncology studies experiences as CRA
- Has more than 2 year of site monitoring experiences
- Good at English reading and writing