Location : Taipei, Taiwan
Our client is dedicated in new drugs research, clinical trial development and production to worldwide.
Take the RD of new drugs as foundation to develop and produce effective and economical drugs.
With strong potential on developing and producing protein drugs and small molecular drugs with high difficulties.
Responsible for both local and global clinical trial management.
Coordinate, monitor and follow up each clinical trial project.
Assist the application of IND, BLA, NDA.
Coordinate with cross function clinical teams and help the budget planing.
Bachelor degree in life science related subjects.
Possess 5+ years of solid experience on clinical operation, especially Phase III trials, and deep knowledge of ICH / GCP.
Known well about the clinical trial related rules of Taiwan, Asia, US and EU pharma markets.
Good communication / coordination skills and high flexibility.
Fluent English in reading and writing.
For more information, please contact Harriet Shih (harriet.shih springasia.com) if interested. Thank you.