our client is a leading global pharma company.

Risk management plans Provision of safety information Implementation of PV
Audit and Inspection Readiness Planning, processing and reporting of
Aggregate Reports to HA and EC (as required) Maintenance of PV Awareness and Training Implementation of Pharmacovigilance Agreements Collection
follow-up and forwarding of spontaneous, literature, solicited, post-marketing
AE cases Submission of single cases to local Health Agencies(HA) and Ethics Committees(as required) Local Market Safety Data Quality

1.Bachelor/Master degree in Science/Pharmacy /Nursing/Medicine
2.3-4 years work experience in Pharmacovigilance(preferably in China)Has a
thorough knowledge of Pv Guidelines and applicable local regulations Essential Skills, Experience, and Competencies
3.Demonstrable strong knowledge of all local PV requirements and of global aspects of drug safety requirements
4.EXcellent verbal and written communication skills with proven ability to negotiate and communicate with internal and external stakeholders