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CRA II at Fortrea - ApplyBlast

CRA II

Fortrea

3 days ago

3.5 on Glassdoor

Santiago, Region Metropolitana, Chile

Onsite

Full Time

Medior

0 applicants

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About this role

The CRA II role involves managing clinical study sites and conducting monitoring visits to ensure compliance with Fortrea's SOPs, ICH GCP guidelines, and sponsor requirements. The position requires safeguarding subject protection and data integrity through source document verification, regulatory document management, and investigational product accountability. This full-time role demands independent site monitoring, travel to study locations, and collaboration with project teams to meet critical study timelines.

Responsibilities

Conduct site monitoring visits including pre-study, initiation, routine, and close-out phases
Verify source data and ensure compliance with ICH GCP guidelines and protocol requirements
Manage investigational product inventory and maintain accurate regulatory documentation

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.