Medical Writing

You will mainly be responsible for the preparation of documents such as clinical trial protocols and reports, as well as drug approval application materials (summary reports, CTD, etc.). The focus will be on molecular targeted drugs and the oncology field. For larger projects like CTD preparation, you will handle one project, and for summary reports, you will be responsible for two or three. Career Path: There are opportunities for transfers to related departments such as line manager, project manager, drug regulatory affairs, and clinical planning. Training System: Basic knowledge can be acquired through e-learning. After that, you will learn the job through practical experience in an on-the-job training format with senior employees. The company has a culture of progressing work collaboratively.

Language Requirements

The above information is a public job ad. This job ad is neither an offer nor a contract.