Location : HsinChu, Taiwan
Our client is focus on research and development on small molecular drugs.
Have their own PIC / S GMP manufactory.
Responsible for planing and writing clinical trial protocols.
Coordinate and monitor the operation of clinical trial.
Review and audit all the clinical trial related documents and reports.
Assist the project assessment.
PhD degree in biochemistry, pharmacy or related subjects.
3+ years research or clinical related working experience.
Experience in drug discovery related IND application is preferred.
Possess solid clinical trial management experience is preferred.
For more information, please contact Harriet Shih (harriet.shih springasia.com) if interested. Thank you.