Site Navigator

Job Overview

Fortrea is seeking a dedicated Site Navigator to support its clinical research operations in Denmark. This role is crucial for ensuring smooth coordination and communication between Fortrea and its clinical trial sites, contributing to the successful execution of studies within the life sciences industry.

Company Overview

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators. Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas. Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes. Together, exceptional is possible. Learn more at Fortrea.com

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: Bachelor’s Degree
• Experience: 3 Year+

Key Responsibilities

• Facilitate effective communication and coordination between Fortrea and assigned clinical trial sites.
• Support site initiation, monitoring, and close-out activities, ensuring adherence to protocols.
• Assist sites with resolution of operational issues and queries in a timely manner.
• Ensure compliance with regulatory requirements and Fortrea’s standard operating procedures.
• Contribute to the overall efficiency and quality of clinical trial conduct in Denmark.
• Maintain accurate documentation and reporting related to site activities.

Requirements

• Bachelor’s degree in a life science, health-related field, or equivalent experience.
• Minimum of 3 years of experience in clinical research or site management.
• Strong understanding of clinical trial processes, GCP, and regulatory guidelines.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently and as part of a global, cross-functional team.
• Proficiency in relevant clinical trial management systems and Microsoft Office Suite.

Benefits

• Opportunity to work with a leading global clinical research organization.
• Contribute to impactful clinical trials transforming patient outcomes.
• Competitive salary and comprehensive benefits package.
• Professional development and career advancement opportunities.
• Collaborative and supportive international work environment.
• Access to cutting-edge technologies and innovative solutions.