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FSP CRA II (Beijing) at Fortrea - ApplyBlast

FSP CRA II (Beijing)

Fortrea

5 months ago

3.5 on Glassdoor

Beijing, China

Hybrid

Full Time

Junior

0 applicants

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About this role

The Clinical Research Associate manages clinical studies by conducting on-site monitoring to ensure adherence to ICH GCP guidelines, regulatory requirements, and sponsor protocols. Responsibilities include verifying data integrity, reviewing informed consent procedures, tracking investigational product inventory, and ensuring audit readiness. The role requires extensive travel to various study sites and collaboration with study teams to meet critical timelines.

Responsibilities

Conduct on-site clinical monitoring visits to ensure protocol adherence
Verify source data accuracy and resolve queries efficiently
Validate informed consent procedures and subject eligibility
Manage investigational product inventory and shipping logs
Ensure site regulatory documents remain current and complete

Skills

Qualifications

Bachelor's DegreeNursing Licensure

About Fortrea

fortrea.com

Headquarters

Lake Park, North Carolina, United States

Company Size

10001+ employees

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Fortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.