- To initiate, monitor and close clinical trials in compliance with study protocol, GCP and SOP
- To manage/resolve study related issues at sites independently
- To develop and maintain good and effective communication with clinical research staff

Requirements:

- 1 years of experience or above on global Clinical trials is a must
- University qualification in pharmacology/pharmacy, healthcare, medicine, biotech or related
- Demonstrated knowledge of, and competence in, application of GCP and ICH guidelines
- Good written and spoken ability both in English (skills at IELTS 6.5 or above, or equivalent)
and Chinese
- Excellent Communication skills
- Love serving clients and traveling
- Result-oriented and can work under pressure
- Good team player