任职要求:
• 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.
岗位职责:
上市后PV工作
负责两次外审工作以及质量支持