Provide Pharmacovigilance (PV) support for patient safety risk management in clinical studies and life cycle management of responsible company product(s)
Partner with cross functional teams for safety reporting
Maintain current knowledge and understanding of regulations, ICH guidelines and industry practices in relation to pharmacovigilance (PV)
Keep abreast of new or changes in local regulations, process and industry practices
Minimum Requirements:
Bachelor degree or above of Medical Science or related field.
Desirable: medical/pharmacological background.
At least 2 years working experience as PV physician or 2 years working experience as senior PV specialist in pharmaceutical company; clinical working experience is preferred
Deep understanding of regulations, knowledge and practices required for pharmacovigilance, e.g. ICH guidelines, international pharmacovigilance regulation, Chinese regulations, industry practice, etc.