Associate Manager, Regulatory Affairs

Responsibilities

• Review product registration dossier and relevant documents
• Obtain IND & NDA approval as well as product registration license renewal as planed
• Coordinate with each function within HMPL from registration pathway
• Establish and maintain relationship with external stakeholders
• Liaise with external stakeholders for regulatory needs of HMPL
• Implement regulatory activities as required by governmental regulations and internal SOPs
• Form accelerate Strategy for product registration

Qualifications

• Bachelor degree and above in Pharmacy or Pharmaceutical
• 5 years or more drug registration experience in pharmaceutical industry
• Prefer oncology drug registration background
• Good understanding of Chinese pharmaceutical & regulatory environment
• Good relation with stakeholders related to product registration
• Fluent English
• Strong communication skill
• Passion in drug development

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