Pl - Associate Director, Clinical Research

leHACK

Clinical research leadership
China regulatory environment expertise
Protocol development and writing
This role serves as the key driver for developing GYN and oncology products towards global registration through innovative clinical research in China

Job Summary

  • This role serves as the key driver for developing GYN and oncology products towards global registration through innovative clinical research in China.
  • The successful candidate will lead strategy development, medical monitoring, and the drafting of study reports and regulatory dossiers.
  • Candidates must possess a PhD or Master's degree with postgraduate training in oncology and deep knowledge of China's clinical development procedures.

Matching Summary

This role serves as the key driver for developing GYN and oncology products towards global registration through innovative clinical research in China.

Skills & Requirements

Must-have

  • Clinical research leadership
  • China regulatory environment expertise
  • Protocol development and writing
  • Key opinion leader engagement
  • Regulatory dossier preparation

Nice-to-have

  • Strategic thinking and flexibility
  • Strong project management skills
  • Parallel task prioritization
  • Resourceful and driven attitude

Key Requirements

  • PhD or Master's in Clinical Medicine (5+ year program)
  • Postgraduate training in Oncology or related major
  • Experience in clinical research and development strategy
  • Fluency in English and Chinese verbal and written

Work Rights

Not specified

Tailored Resume

Cover Letter