Responsibilities：
- 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
- Supervise junior CRAs
Requirements:
- University qualification in pharmacology/pharmacy, healthcare, medicine, biotech or related
- 3 years of experience or more of conducting global clinical trials
- Project management experience preferred
- Demonstrated knowledge and competence in, application of GCP and ICH guidelines
- Very good written and spoken ability both in English (skills at IELTS 7.0 or above, or equivalent) and Chinese
- Excellent Communication skills
- Love serving clients and traveling
- Result-oriented and can work under pressure
- Good team player