Basic purpose of the job*
Independently writes and manages global and/or local clinical documents required for advancing clinical development programs in global and/or local, cross-functional project and/or trial teams, with the ultimate goal of creating value for patients in need. Provides critical input to the analysis and interpretation of clinical data in the assigned writing projects. Oversees writing assignments of external medical writers. Contributes to process improvements and working groups with cross-functional impact.

Requirement ：
1.Prefer to Master degree in life science or other；
2. Highly proficient in both spoken and written English；
3. At least one year work experience in clinical research or pharmaceutical industry