Fortrea

Verified Job Source

Bringing life-changing benefits to patients faster

Research Triangle Park, NC

Biotechnology Research

5,001+ people

About

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

Open positions

Clinical Trial Manager

Remote

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. Remote US or Canadian based. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments. The role generally works under the direction of a (Senior) Clinical Trial Manager, however,…

FSP Clinical Research Associate 2 - Oncology

Remote · United States

Responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. Ensures patient protection, protocol adherence, and data integrity while managing site activities and reporting serious adverse events.

FSP Clinical Research Associate 2 - West, Central, and South Regions - Oncology

Remote · Durham, California, United States, Oconee County, South Carolina, United States, West, West Virginia, United States

The Clinical Research Associate is responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. They also ensure the protection of study patients, verify protocol adherence, and maintain the integrity of data submitted on Case Report Forms.

Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal

Hybrid · Montréal

The Clinical Trial Coordinator serves as the primary contact for investigative sites, managing site performance, regulatory documentation, and study supply distribution. They are also responsible for processing site invoices, managing payments, and ensuring compliance with study protocols and financial requirements.