1. Be responsible for domestic and foreign preclinical registration work according to the company's requirements.

2. Support clinical tests of new drugs.

3. Be responsible for examining the integrity and authenticity of corresponding project materials and communicate with CROs.

4. Coordinate pharmaceutical, preclinical and clinical registration applications and communicate with registration institutions. 

5. Be responsible for formulating, improving and upgrading the SOP of the new drug coordination department and report it to leaders for examination and approval. 

6. Cooperate with other departments in project research and consultation. 

1. Be familiar with drug registration in main countries and regions, conduct technical checks on application materials and hold a Master’s Degree or above.

2. Majored in those related to pharmacy, pharmacology, biological pharmacy, molecular biology and cell biology. (Give priority to those having experience in research and development of nucleic acid drugs or registration.)

3. Have more than three years of relevant work experience in scientific research institutions, pharmaceutical companies or CROs. 

4. Read and write English fluently.