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 · 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 · 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.
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.
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.