Clinical Research Associate I – Site Monitoring (Beijing)

About the role

The Clinical Research Associate I will be responsible for monitoring and managing clinical trial sites in Beijing, ensuring compliance with study protocols, regulatory guidelines, and sponsor SOPs. This role involves on‑site visits, data verification, and coordination with internal teams and external vendors.

Key responsibilities

• Conduct routine site monitoring, pre‑study, initiation, and close‑out visits.
• Maintain study files, ensure informed consent procedures, and verify protocol adherence.
• Review source documents, verify data integrity on CRFs, and query missing or implausible data.
• Prepare accurate trip reports and manage travel expenses in line with Fortrea policy.
• Act as the primary contact for clinical trial supplies and vendor coordination.
• Support registry management, feasibility assessments, and quality‑control visits.
• Assist senior CRA with site budget management and SAE reporting.
• Perform CRF review, generate queries, and resolve data issues using Fortrea or client data systems.
• Mentor new monitors and coordinate local project activities as needed.

Required profile

• University or college degree, or certification in a related allied health profession from an accredited institution.

Required skills