CRA I

Fortrea Holdings Inc.

Job Overview

Location

Remote Belgium

Job Type

Full-time

Full Job Description

📋 Description

• Join Fortrea as a Clinical Research Associate I and contribute to the delivery of high‑quality clinical trials that make a real difference in patients’ lives. This role offers an exciting opportunity to build your monitoring expertise while working in a dynamic, global life sciences environment that drives innovation and advances healthcare worldwide.
• You will conduct all aspects of study site monitoring, including routine visits, initiation, and close‑out activities; oversee site management activities in alignment with project plans and SOPs; ensure study staff are properly trained and equipped to conduct the protocol safely and accurately; safeguard patient safety by verifying informed consent and adherence to protocol and regulatory requirements; review source documentation to ensure data integrity and identify missing or inconsistent data; manage monitoring tasks efficiently and in line with Fortrea policies, including economical travel planning; maintain audit‑ready site documentation; prepare clear and timely monitoring visit reports; collaborate with internal teams to assess project needs, timelines, and resources; act as a point of contact for clinical trial supplies and assigned vendors; participate in feasibility assessments, QC visits, and registry management tasks; support activities such as investigator recruitment, EC submissions, regulatory notifications, and meeting organization; follow up on Serious Adverse Events (SAEs), including report processing and narrative review; review CRFs, generate queries, and resolve data issues according to guidelines; may mentor and co‑monitor with new team members; may coordinate assigned clinical projects locally and act as the point of contact for the client where applicable; and perform other duties as assigned.
• Fortrea is a global life sciences organization dedicated to advancing healthcare through innovative clinical research. The company operates with a mission-driven culture focused on patient safety, data integrity, and the successful delivery of impactful research programs across therapeutic areas.
• In this role, you will build deep expertise in clinical trial monitoring, strengthen your understanding of regulatory frameworks (such as ICH-GCP), develop cross-functional collaboration skills, and gain hands-on experience managing end-to-end site activities. You will have opportunities to grow your career within a global organization, supported by wellness programs, learning resources, and employee resource groups, while contributing to meaningful research that improves patient outcomes.

🏖️ Benefits

• Opportunities to grow your career in a global clinical research environment
• Collaborative and inclusive culture supporting your professional development
• Access to wellness programs, learning resources, and global ERGs
• Competitive benefits tailored to your local market

Skills & Technologies

Remote

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Fortrea Holdings Inc.

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About Fortrea Holdings Inc.

Fortrea is a global contract research organization spun out from LabCorp in 2023 to provide drug development services across Phases I-IV. It offers clinical trial management, patient access solutions, regulatory consulting, and commercialization support to biopharmaceutical, medical device, and diagnostic clients. The company operates in more than 90 countries with 19,000 employees, leveraging therapeutic expertise in oncology, rare diseases, neuroscience, and other complex areas to accelerate therapies from lab to market while prioritizing patient experience and data-driven insights.

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