Bringing life-changing benefits to patients faster
Research Triangle Park, NC
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
Remote · Canada
The Senior Clinical Data Manager leads end-to-end data management activities for oncology studies, ensuring quality, timelines, and budget adherence. They provide mentorship to junior staff, manage sponsor relationships, and oversee the implementation of study-specific data procedures.
Remote · Canada, Mexico, United States
The Clinical Team Lead manages the clinical delivery of research trials, acting as the project lead to ensure adherence to timelines, budgets, and quality standards. They are responsible for driving project performance, managing clinical risks, and fostering collaboration within a matrixed, multicultural team environment.
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 budget and scope. They drive project performance, manage clinical risks, and lead cross-functional teams in a matrixed environment.
Remote · Canada, United States
The Senior Clinical Scientist leads Phase 1-3 clinical trials and oversees medical monitoring activities, including protocol design and endpoint development. They serve as the primary scientific point of contact for internal and external stakeholders and manage the execution of clinical trial protocols.
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.
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.
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.
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.
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.
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…
Remote · Canada
Responsible for all aspects of clinical site monitoring, including routine visits, close-outs, and site management. Ensures data integrity, patient protection, and adherence to study protocols and regulatory requirements.
