Clinical Research Commissioner

 According to ICH-GCP requirements, the organization responsible for drug clinical trials, implementation, implementation and clinical audit
* According to research programs and project plans to ensure the operation of the implementation of high quality clinical project
* Responsible for organizing the meeting clinical trial investigators, and research units to maintain good communication and coordination
* According to ICH-GCP and project requirements, the proper establishment and management information system project file
* According to the company needs to provide the necessary technical support related to clinical trials
Requirements
1. Integrity, dedication, hard work, steadfast;
2. Medical or pharmacy related majors, college degree or above
3. For clinical audit work has a strong interest in clinical audit relevant experience preferred;
4. Good communication and coordination ability, ability to handle customer relationship
5. Skilled use of common office software, including word, excel, powerpoint, etc.
6. English 4 or more
7. Strong ability to work independently and team spirit
8. Good physical condition, able to adapt to high-intensity work to travel frequently