With strong capability to identify, select, initiate, conduct and close-out appropriate trial sites for clinical studies. Monitor those sites through managing CRO staff in order to ensure that the studies are carried out according to the protocol, Chugai SOPs, applicable regulations and the principles of ICH-GCP.
With line manager’s guidance, to coordinate and manage the activities of individual studies and site/CRO staff in a manner that ensures all timeframes and targets are met and that costs are kept under control.
With line manager’s guidance, to effectively manage assigned CRO staff to ensure high performance, continuous development, and low turn-over.
With line manager’s guidance, to work as the contact person in China for global clinical development consolidation system 1) installation task force formed in Chugai headquarters in Japan.

1.University/Bachelor’s degree or equivalent degree/experience and a background in medicine, pharmacy, science or other relevant disciplines.
2.A satisfactory progression of monitoring experience with some experience in leadership and/or management activities and relevant experience for two to five years.
3.Fluent in written and spoken English. TOEFL score higher than 90, CET-6 or equivalent. (Overseas educational background in English speaking countries desirable.)
4.Basic computer literacy. (High computer literacy desirable.)
5. Highly developed problem solving and cross-cultural communication skills, and keen to learn new things