Basic Function：
1.To perform clinical monitoring activities of designated projects in accordance with the Parexel's SOPs (or the Sponsor’s SOPs as appropriate), which include: investigator/site selection, managing and coordinating site related activities, collating regulatory documentation and IRB submissions, and monitoring activities (such as source data verification, drug accountability, etc.) throughout the study in accordance with the ICH GCP guidelines.
2.Also accountable for detecting, analyzing and solving technical, procedural and/or motivational problems that may occur to the site staff of the investigation team and thus affect the progress of the project.
3.Supporting local issues like SSU, project local issues; monitoring within the region.
Requirement and Qualification:
1.A bachelor (or above) degree in a life science (preferably paramedical) field.
2.More than 2 years’ work experience in clinical operations, particularly study monitoring.
3.Good communication skill and proactive attitude.
4.Ability to take initiative and work independently.
5.Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English.
6.Ability to travel – on both local and international trips.