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CRA 2 at Fortrea - ApplyBlast

CRA 2

Fortrea

4 months ago

3.5 on Glassdoor

Bangkok

Hybrid

Full Time

Junior

0 applicants

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About this role

A Clinical Research Associate at Fortrea is responsible for site management and monitoring of clinical trials in accordance with SOPs, ICH GCP guidelines, and sponsor requirements. This role involves ensuring subject protection, maintaining data integrity through source document verification, and managing investigational product inventory while performing routine and close-out site visits. The candidate will work across clinical research units, hospitals, and office environments, often requiring significant travel to study sites.

Responsibilities

Monitor clinical study sites according to standard operating procedures and ICH GCP guidelines.
Verify informed consent procedures and protocol requirements to ensure subject protection.
Perform source data verification and resolve queries to maintain data integrity.
Manage investigational product inventory and ensure accurate storage per protocol.
Track and follow up on serious adverse events as assigned by management.

Skills

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.