1.Collect drug registration laws and regulations, variety trends, understand the current situation of the industry;

2. Assist in writing, sorting, internal review and archiving of registration application dossiers;

3. Communicate with drug regulatory authorities to follow up the registration progress;

4. Coordinate and communicate the progress of registration project;

5. Assist in preparing relevant materials and documents according to the requirements of on-site drug inspection;

6. Completing other tasks assigned by leaders in a timely manner.

1. Bachelor degree or above in pharmacy, medicine, English, biopharmaceutical or related majors,

2. Proficient in literature review, sorting and analysis, good logical thinking ability and copywriting ability;

3. Good English skills in listening, speaking, reading and writing, CET-6 is preferred;

4. Actual experience in or responsible for the application of biological new drugs, prior experience in the application of cellular drugs or genetic drugs.