Pl - Associate Director, Clinical Research

Merck & Co., Inc.

Clinical research leadership
China regulatory environment knowledge
Study protocol development
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.
  • The position requires a PhD or Master's degree in clinical medicine with deep expertise in the China regulatory landscape and 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 knowledge
  • Study protocol development
  • Regulatory dossier preparation
  • Key opinion leader engagement

Nice-to-have

  • Strategic project management skills
  • Fluent English and Chinese communication
  • Experience with parallel task prioritization
  • Resourceful and flexible mindset

Key Requirements

  • PHD/Master in clinical medicine
  • Postgraduate training in oncology
  • 5-year medical school graduates
  • Previous clinical research experience
  • Fluency in English and Chinese

Work Rights

Not specified

Tailored Resume

Cover Letter