Ii. Medical writing

Job responsibilities:

1. Responsible for literature retrieval and information extraction of clinical trials;

2. Responsible for the writing of clinical trial programmes, research manuals and other related materials;

3. Responsible for medical support for clinical trials;

4. Responsible for the formulation of relevant SOP;

5. Other work assigned by the company.


1. Major in clinical medicine, pharmacy, bachelor degree or above;

2. Strong language and communication skills;

3. Retrieve and read English literature materials without obstacles;

Basic knowledge of GCP and relevant laws and regulations

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