1.Medical Aspect
•Provide scientific support to product value and long term development.
•Develop sale team medical capability through medical training, lecture delivery and medical knowledge update through various channels.
•Enhance the delivery of new concept and products key message to key influencers/stakeholders, and establish cooperation and partnership with medical association to promote medical advancement.
•Provide medical expert opinion in safety events management to avoid negative impact
•Review promotion material documents, ensure company’s medical compliance.

2.Pharmacovigilance Aspect
•Organize, manage, and carry out local PV activities, such as adverse event monitoring, safety reporting, risk management, local safety monitoring activities as required by local agency, local PV contractual agreements, process documentation and training, etc.
•Collect all adverse events for all Sandoz products from clinical trials, post-marketing studies, Spontaneous Reports, registries, commercial programs, etc.
•Ensure processed cases to verify accuracy, consistency, and compliance with process requirement.
•Ensure complete and timely forwarding of ICSR to Argus system and to local Health Authorities according to GOP and local regulations requirements.
• Prepare line listing of imported products, and ensure timely submission according to local HA requirement.
•Ensure timely preparation and submission PSUR of imported products and locally products
•Process literature cases detected locally.
•Develop and update training materials for Pharmacovigilance and ensure training of associates on relevant PV procedures and in ADR/AE reporting, and to ensure clear, correct and complete documentation of all training.
•Survey and monitor national PV regulations.
•Management and maintenance all local relevant PV databases.

知名外资医药公司，产品行业竞争力强，企业内部环境宽松，工作量适中，内部晋升空间充足，薪水处于行业前端水平