1. Assist the clinician with the non-scientific judgments of international multi-center clinical trials in compliance with GCP and the protocol;

2. Assist in the screening, enrollment, and follow-up visit of subjects;

3. Assist in collecting, archiving and management of study materials;

4. Input clinical data into clinical trial system(operating system in English).


1. Junior college or above in medical science, nursing or related subjects, foreign nursing specialty will be a plus;

2. Minimum 1 year of experience as a CRC or working in clinical circumstances; clinical trial experience will be a plus;

3. CET 4 or above in English, and good command of English listening& speaking& reading & writing;

4. Ability to work independently, with a team spirit;

5. Ability in working under pressure and self-regulation;

6. Positive work attitude, good communication skill and adaptability to change, and strong self-learning ability;


Work area :Beijing Shanghai Guangzhou Chengdu Chongqing Tianjin Changchun Hefei Fuzhou

Changsha Wuhan Hangzhou Harbin


Photo-number:021-6075 5800




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