Pl - Associate Director, Clinical Research

Merck & Co., Inc.

Gyn program leadership
China regulatory environment expertise
Study protocol development
The role serves as the key driver for developing products towards registration with a focus on innovative clinical research in China

Job Summary

  • The role serves as the key driver for developing products towards registration with a focus on innovative clinical research in China.
  • Candidates must possess a deep understanding of the China regulatory environment and clinical development procedures to facilitate global drug development.
  • The position requires strong project management skills to handle multiple tasks while engaging key opinion leaders and drafting study reports.

Matching Summary

The role serves as the key driver for developing products towards registration with a focus on innovative clinical research in China.

Skills & Requirements

Must-have

  • GYN program leadership
  • China regulatory environment expertise
  • Study protocol development
  • Key opinion leader engagement
  • Regulatory submission dossier preparation
  • English and Chinese fluency

Nice-to-have

  • Strategic thinking and flexibility
  • Parallel task prioritization
  • Persistent and resourceful attitude
  • Medical monitoring experience
  • Team leadership capabilities

Key Requirements

  • PhD or Master in Clinical Medicine (5-year medical school)
  • Postgraduate training in oncology or related major
  • Previous clinical research and development experience
  • Fluent verbal and written English and Chinese
  • Willingness to work outside primary medical specialization

Work Rights

Not specified

Tailored Resume

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