Fortrea

Core ICF Developer/Writer and Reviewer (Centralized role)

Fortrea

1 year ago
Mexico City, Mexico
Hybrid
Full Time
Senior
0 applicants
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Fortrea
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About this role

A clinical documentation specialist focused on informed consent forms and related clinical trial documents, ensuring they are accurate, compliant, and understandable for research participants. The role sits within clinical research to align consent content with study protocols, client requirements, and applicable regulatory frameworks. It also supports development of master templates and training materials to maintain document quality and consistency.

Skills

Qualifications

University/College Degree (Medical Preferred)
Fortrea

About Fortrea

fortrea.com

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.

About Fortrea

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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