Responsibilitie********
1、 To develop clinical trial protocols, clinical study report withproject team
2、 To design CRF/SD an******** study document
3、 To translate medical files
4、 To search an******** relevant medical literatures
5、 To develop an******** goo******** with clinical experts
6、 To provide medical advice on registration issue
岗位要求:
Qualification********
1、 Medical/Pharmacological Master degree or Ph.D.
2、 ≥2 years of experience with scientific research metho********including designing an******** exper******** an******** an********experimental results
3、 Experience with scientific writing (publications in both Chinesean******** journals or equivalent)
4、 Understanding of drug development process an******** guidelines
5、 Goo******** skills for both Chinese an********
6、 Basic knowledge of biostatistics
7、 Goo******** skills
8、 Ability an******** to plan an******** on complex tasks, multiple tasks
9、 Ability to work effectively as a team player as well as independently.