Nasdaq:US$36.56 (-0.93) | HKEX:HK$57.55 (-1.15) | AIM:£5.35 (-0.03)
人才招募
上一篇文章   |   下一篇文章
临床及注册, 北京 | 2020-05-11

高级注册经理

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