Responsibilities:
1. Provide support to clinical trial-associated documents for new and ongoing programs,including but not limited to CRF，CSR，IB
2. Being familiar with all quidelines and regulatory requirements related to regulatory medical writing(e.g. ICH-GCP, NMPA)
3. Coordinate and manage review cycles, incorporates team comments and lead discussions on document revision and finalization
Qualification:
1. Bachelor or Master degree preferably in medical sciences or other relevant fields
2.1-2 years of medical writing/ translating experience,oncology field preferred
3.Excellent verbal and written English/ Chinese Language skills, understanding of clinical research,the drug development process