Pl - Associate Director, Clinical Research

Merck Sharp & Dohme Corp

Deep understanding of china regulatory environment
Experience in clinical trial planning and monitoring
Fluent english and chinese verbal and written skills
This role serves as the key driver for developing GYN and oncology products towards registration in China

Job Summary

  • This role serves as the key driver for developing GYN and oncology products towards registration in China.
  • The successful candidate will lead study protocol development, engage key opinion leaders, and prepare dossiers for regulatory submission.
  • The position requires a PhD or Master's degree with postgraduate training in oncology or a related major.

Matching Summary

This role serves as the key driver for developing GYN and oncology products towards registration in China.

Skills & Requirements

Must-have

  • Deep understanding of China regulatory environment
  • Experience in clinical trial planning and monitoring
  • Fluent English and Chinese verbal and written skills

Nice-to-have

  • Bright, driven, and strategic mindset
  • Strong project management and prioritization skills
  • Resourceful and flexible approach to tasks

Key Requirements

  • PHD/Master in clinical medicine (5-year medical school graduate)
  • Postgraduate training in oncology or relative major
  • Previous experience in clinical research/development strategy

Work Rights

Not specified

Tailored Resume

Cover Letter