Clinical Trial Reg Affairs Specialist III
Thermo Fisher Scientific
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Responsibilities:
Be responsible for the registrations of imported drug. Including but not limited to the good communications with NMPA, CDE and other authority, registration documents preparation, performing the test, documents submissions and follow up of NMPA until get the approval. Timely documents archiving. Other tasks if needed.
Minimum Qualifications: Bachelor degree
At least 2-3 year’s experience on imported drug registration
Good at written and oral English
Preferred Qualifications: Medical education background
The experience on all of API, ANDA, IND and other type registration is preferred
Good communications skill
Have experiences at global pharma is preferred.
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