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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

Site Budgeting and Contracting Specialist - FSP

Remote · Canada, United States

The specialist is responsible for preparing country site budgets, managing clinical trial agreement negotiations, and ensuring all financial exhibits are executed in compliance with legal standards. They will also act as a primary liaison between clinical trial sites, legal departments, and internal clinical operations teams to facilitate study start-up and ongoing budget maintenance.

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

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.

Senior Clinical Project Manager, Phase I

Remote · Canada, United States

The Senior Clinical Project Manager oversees domestic and global projects, ensuring delivery within scope, schedule, and budget while maintaining quality standards. They also lead project teams, manage client relationships, and provide line management and technical support to staff.

FSP Clinical Research Associate 2 - Central Region

Remote · Durham, California, 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 through careful source document review and site management.

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.

Clinical Operations Manager (COM)

Hybrid · Montréal

The Clinical Operations Manager is responsible for the execution and oversight of local clinical trial activities, including regulatory compliance and financial management. They must effectively manage study start-up, site budgets, and local submissions while collaborating with internal and external stakeholders.

FSP - Clinical Team Lead - Ophthalmology - US & Canada

Remote · Canada, United States

The Clinical Team Lead owns the clinical delivery of research trials, functioning as the project manager to ensure successful execution within contractual and budgetary requirements. They drive project performance, manage clinical strategy, oversee site monitoring, and lead high-performing teams in a matrixed environment.

Senior Clinical Project Manager, Phase I

On-site

Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5+ years of global project management experience, with mandatory experience in phase I. Candidates must be based in the United States or Canada. Job Overview: At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance fr…