I joined MIMS in Feb 2018 while MIMS launched TW branch. In the beginning, I supported not only project management, but TW office set up, and grew the business successfully. Afterwards, I focused on the project management, and helped clients to complete many complicated projects, including veeva projects.

In Elsevier, I was responsible for manage projects from pharmaceutical company, coordinate with marketing and medical departments. The projects are varied, such as conferences, e-content and platform, printed materials, commercial and academic communication tools, etc. The challenge is you do not know what client want you do, however, it is also why I can do many kinds of projects.

Be responsible for finishing clinical trial document: ICF, CSR, etc. Be familiar with new drug development, ICH, and GCP.

Be responsible for publishing management and communication.

Be responsible for proposal, medical writing, medical editing, project management, communication, and production. Be familiar with pharmaceutical industry.

Laboratory of Free Radical Biology, School of Medical Technology