上市后PV工作 负责两次外审工作以及质量支持

• Sound knowledge of general medicine or pharmacy and clinical practice, scientific/life-science background, medicinal knowledge preferred; proficiency in medical terminology (local languages). • Proven ability to organize workflow activities and manage multiple critical issues. • Computer literate with basic knowledge of GMS database systems. • Awareness of and familiarity with industry principles of drug development and pharmacology • Proficiency in global and local SOPs. • Good verbal and written communication skills, fluency in local language(s) and English language required. • Ability to negotiate and communicate with internal and external customers. Ability to establish and maintain open relationships within the organisation and with authorities. • Demonstrable knowledge of all local PV requirements and of Global aspects of drug safety. Experience • Scientific study and experience in pharmaceutical regulations and R&D processes. • Pharmaceutical industry experience including a PV responsibility role required.