Overview

We are currently looking for a Clinical Research Associate based in the Helsinki area with at least 2 years of independent monitoring experience and a willingness to work across multiple sponsors. This is a great opportunity to join Fortrea and contribute to high-quality clinical trials, supporting diverse studies while ensuring compliance, data integrity, and patient safety at every stage.

Responsibilities

• Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
• Conduct site monitoring responsibilities for clinical trials according to Fortrea’s SOPs, ICH guidelines and GCP; including Pre‑study, Site Initiation, Process Monitoring, Routine Monitoring, and Close‑out Visits.
• Prepare and implement project plans related to Clinical Monitoring responsibilities. ...