Deep understanding of china regulatory environment
Fluent in english and chinese verbal and written
This role serves as the key driver for developing products towards registration within GYN programs in China
Job Summary
This role serves as the key driver for developing products towards registration within GYN programs in China.
The successful candidate will be responsible for developing study protocols, engaging key opinion leaders, and preparing dossiers for regulatory submission.
The position requires a deep understanding of the China regulatory environment and clinical development procedures to facilitate global drug development.
Matching Summary
This role serves as the key driver for developing products towards registration within GYN programs in China.
Skills & Requirements
Must-have
Project lead for GYN programs
Deep understanding of China regulatory environment
Fluent in English and Chinese verbal and written
Nice-to-have
Bright, driven, dedicated, persistent personality
Strategic and flexible approach to work
Resourceful with strong leadership skills
Key Requirements
PHD or Master in clinical medicine (5-year medical school graduate)
Postgraduate training in oncology or related major
Previous experience in clinical research strategy and protocol writing