MAIN REPONSIBILITIES:  Discuss the study protocol with the investigators.  Review and approve patient enrollment.  Review protocol compliance and manage protocol deviation.  Study medical data review  Serious adverse event review and follow up.  Managing queries from the clinical site staff  Provide medical opinion/review in the clinical study reports.  Draft clinical studies summary and overview QUALIFICATIONS:  Bachelor’s degree in clinical medicine is essential, and MD/PhD is preferred.  At least 5 year working experience in clinical medicine is must.  At least 5 years working experience in clinical development function of global biopharmaceutical industry is must.  Strong leadership, excellent communication, and project management skill.  Excellent in both English and Chinese.