岗位职责：
Responsibilities:
1、 To develop clinical trial protocols, clinical study report with project team
2、 To design CRF/SD and other study document
3、 To translate medical files
4、 To search and summarize relevant medical literatures
5、 To develop and maintain good relationship with clinical experts
6、 To provide medical advice on registration issue

岗位要求：
Qualifications:
1、 Medical/Pharmacological Master degree or Ph.D.
2、 2 years of experience with scientific research methodology, including designing and conducting experiments, and analyzing and reporting experimental results
3、 Experience with scientific writing (publications in both Chinese and English journals or equivalent)
4、 Understanding of drug development process and regulatory guidelines
5、 Good writing skills for both Chinese and English
6、 Basic knowledge of biostatistics
7、 Good communication skills
8、 Ability and flexibility to plan and prioritise on complex tasks, multiple tasks
9、 Ability to work effectively as a team player as well as independently