Description of position:
1. Participate in pharmacovigilance related meetings and trainings organized by drug regulatory departments and other administrative departments, and timely transmit the meeting spirit of national and local drug regulatory departments to the company headquarters
2. Conduct training for internal and external personnel
3. Responsible for the collection, evaluation and report of adverse drug reactions/events through various channels
4. Responsible for ADR report and monitoring document management
5. Organize, supervise and coordinate internal departments or external experts to evaluate, investigate and report group adverse events and death cases, and cooperate with drug regulatory departments, health administrative departments and ADR monitoring institutions to investigate
6. Prepare periodic safety update report (PSUR) and ADR monitoring data verification and analysis report
7. Establish good relationships and close cooperation with health regulatory authorities and institutions, clinical experts and statistical experts

Requirements for Employment：
1. Bachelor degree or above in Medicine, pharmacy, epidemiology, etc., working experience is preferred
2. Master professional knowledge of medicine, pharmacy, nursing, epidemiology or statistics, and have the ability to investigate, analyze, evaluate and report adverse drug reactions
3. Familiar with ADR reports and monitoring documents; Familiar with medical literature retrieval methods