Chief Medical Officer

15 hours ago

Taipei Taipei City, Taiwan RGP Full time $104,000 - $130,878 per year

Purpose of the role:

The successful candidate will review and design clinical protocols, monitor clinical trials, and communicate with international regulatory agencies. Position title is negotiable and will be commensurate to relevant experience.

Responsibilities:

  • Critically review and revise clinical trial protocols
  • Serve as primary communicator with Clinical Trial CRO providers and regulatory authorities
  • Identify and communicate with local and international KOLs in therapeutic indications related to company programs
  • Identify and engage with consultants and CROs for services related to company program
  • Generate and make presentations on behalf of the company at external meetings and conferences
  • Foster collaborative relationships with employees both within and outside the company

Technical requirements:

  • Command a deep understanding of company programs and keep current with latest relevant scientific research and development
  • Generation and review of technical reports and presentations
  • Ability to search and survey the technical literature using online tools

Minimum qualifications:

  • Doctor of Medicine (M.D.) or PhD in clinical sciences, or equivalent combination of education and experience
  • Clinical trial experience in
    oncology
  • Ability to communicate in written and spoken English and Chinese

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