1.Understand GCP and SOP to support CRA or PM to prepare, collect and maintain study documents, review in-house documents, tidy up and archive documents at eTMF

2.Support CRA or PM to supply and deliver materials and non-drug supply related to trial execution

3.Assist site payment and tracking

4.Provide logistic support for Investigator Meeting, AB board meeting or KOL meetings etc.

任职资格：

1.Bachelor's degree in a health care or other scientific discipline or educational equivalent,

2.Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

3.Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer

4.Good written and verbal communication skills

5.Good organizational and problem-solving skills

6.Effective time management skills

7.Ability to establish and maintain effective working relationships with coworkers, managers

上班地址：上海市徐汇区银都路466号2号楼1楼