
Clinical Research Associate
1 week ago
ResponsibilitiesWhat 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
- In charge of oncology projects
- Bachelor degree or above
- Has more than 1 year of solid site monitoring experiences in Taiwan (The title will be finalized by the MV experience)
- Good at English reading and writing, Proficiency in Chinese
- Must located in Taiwan
- Working location: Taipei office with 2 days flexibility to WFH
ICON
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