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FSP CRA II（Wuhan） at Fortrea - ApplyBlast

FSP CRA II（Wuhan）

Fortrea

3 months ago

3.5 on Glassdoor

Shanghai, China

Hybrid

Full Time

Junior

0 applicants

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About this role

This role involves managing clinical study sites and conducting monitoring visits to ensure adherence to ICH GCP guidelines, regulatory requirements, and company SOPs. Key duties include verifying informed consent procedures, safeguarding data integrity through source document reviews, managing investigational product inventory, and ensuring audit readiness. The position requires independent travel to study sites to oversee protocol execution and maintain data accuracy across various clinical trial phases.

Responsibilities

Conduct site monitoring visits for clinical trials according to SOPs and GCP guidelines
Verify informed consent procedures and protocol adherence to protect study subjects
Ensure data integrity through source document review and query resolution
Manage investigational product inventory and accountability per protocol requirements
Prepare and implement study-specific monitoring plans and site initiation slides

Skills

Qualifications

Nursing LicensureLife Science Qualification

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.