RA Manager (3 persons) 2024-12-12

Responsibilities: 1. Review, draft or prepare drug registration documents to ensure the quality of application materials; 2. Be responsible for the submission of registration documents, track the progress of the review, deal with all kinds of common problems encountered in the registration inspection and issuance of supplementary replies at any time; 3. Provide consultation on regulations related to drug registration for customers and company projects. 4. As a mentor, provide technical guidance and training to RA Managers and specialists. 5. Perform other tasks assigned by the supervisor.