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Clinical Research Associate

Caidya · China, China, China

Location
China
Job Type
Full-time
Posted
June 13, 2026

Job Description

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...

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