Overview:

Responsible for the clinical trials and performance studies conducted in China. Meanwhile, responsible for the communication and cooperation with manufacturers about oversea clinical studies and data acceptance.

Responsibilities:

• Registration clinical trials which is conducted in China;
• Clinical evaluation which is for registration;
• Performance studies which is conducted in China;
• Communication with divisions and global team on China clinical trial requirements;
• Cooperation with divisions on oversea clinical data acceptance, and clinical trials which are for both oversea countries and China registration.

Qualifications:

• Bachelor degree at least with the major of medicine or biology. Master or doctor degree is preferred. Clinical examination is preferred.
• At least 5 years clinical trial experience in international IVD companies. Leading team is preferred.
• Be able to travel frequently (twice a month at least).
• Good at communication. Good oral and written English.

上班地址：酒仙桥路10号 恒通商务园