职位： 临床事务经理

1. 有海外工作、学习经历
2. 本科其以上学历，5年以上相关工作经验
3. 4个月内到位

Main responsibilities:
-To ensure a smooth communication between the company and sites, company and CRO, report any studies related issues to clinical trial manager in a timely manner.
-To conduct site co-monitoring with CRO company.
-To initiate,monitor and close up clinical trials in compliance with study protocol,ICH-GCP & SOPs.
-To report all Adverse Events timely and properly according to company's SOP.
-To manage Investigational Product in compliance with protocol and the company's SOP.
-To organize investigator meetings.
-To provide on-site training.
-To document and archive all clinical trial relevant activities.

Qualifications:
Medical Bachelor degree or above in related field (medicine or pharmacy science)
At least 1~3 years clinical trial experiences working in multi-national pharmacy company or CRO company
Familiar with China SFDA regulations,ICH-GCP guidelines and clinical trial design and conduction
Excellent verbal and written communications skills in both Chinese and English
Ability to work independently
Ability to work on a multidisciplinary team
Good interpersonal skills,negotiation skills and presentation skills
Good computer skills
Willing to travel frequently