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.
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