Full-time

Clinical Research Associate I

Posted by Caidya • Shanghai, Shanghai, China

📍 Shanghai, Shanghai 🕒 March 03, 2026

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About the Role

Job Overview:
The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines, ISO14155 and other applicable regulations. Builds, manages and supports site relationships while serving as liaison between the Sponsor and assigned sites.
Job Duties and Responsibilities:
Provides support to Project Team and Clinical Operations Team.
Maintains working knowledge of protocols and Monitoring Plans for assigned projects.
Demonstrates good written and verbal communication skills.
Serves as primary contact for assigned research sites.
Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
Responsible for scheduling and conduct of pre-study visits, initi...
                

Job Details

Location Shanghai, Shanghai
Job Type Full-time
Category Life Scientists
Posted March 03, 2026
Deadline April 12, 2026

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