Clinical Affairs Specialist
Thermo Fisher ScientificShanghaiUpdate time: August 8,2019
Job Description
Job Description
- As a CRA to manage the site, including but not limited to site selection, Ethic's committee review, study agreement signing, investigator meeting, enrollment, trial master file management, site monitoring, source data verification and site close-out;
- As a CRA to on site manage and track the study timeline, study budget and products of company sponsored studies;
- Ensuring the clinical studies are in compliance with local regulations, GCP and Thermo SOPs;
- Establishing and maintaining the good relationship with investigators and sites.
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