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Clinical Research Associate I

Caidya
Full-time Shanghai, Shanghai Life Scientists
Posted:
March 02, 2026
Location:
Shanghai, Shanghai, China

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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    Job Overview

    Job Type: Full-time
    Location: Shanghai, China
    Posted: March 02, 2026
    Deadline: April 11, 2026