Responsibilities:

- To manage/resolve study related issues at sites independently and keep it in compliance with study protocol, GCP & SOP
- To develop and maintain good and effective communication with clinical research staff & sponsor representative

Requirements:

- University qualification in nursing, pharmacology/pharmacy, medicine, biotech or related.
- 1 years of experience or above on clinical trials & site management
- Demonstrated knowledge of, and competence in, application of GCP and ICH guidelines
- Good written and spoken ability both in English and Chinese
- Excellent Communication skills
- Love serving
- Result-oriented and can work under pressure
- Good team player