Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary Of Responsibilities Responsible for all
Fortrea is seeking a Senior Clinical Research Associate to lead site monitoring and site management for multicenter clinical studies in Italy. You will ensure adherence to company and sponsor SOPs, regulatory guidelines, and study plans, while coordinating
Fortrea seeks a Site Start-Up Specialist to coordinate start-up activities, manage essential documents, and ensure timely regulatory submissions. You will join the FSPx team and work with a renowned sponsor to advance development of innovative therapies. In
Join Our Team and Shape the Future of Clinical Research! At Fortrea , we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist, you will play a
Fortrea in Turbigo, Italy is looking for a Site Budget & Contract Specialist to streamline clinical trials and ensure compliance with global regulations. In this role, you will negotiate site agreements and manage budgets to support innovative
Clinical Research Associate II - Full Service Operations Model - Italy Fortrea Research Associate Posted Aug 2026 About this position Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard
Fortrea seeks an experienced Clinical Research Associate II for Italy to oversee site monitoring and site management for multicenter studies. You will ensure adherence to regulatory guidelines, manage study files, and support initiation and closeout visits with
Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA
Fortrea in Italy is seeking a Senior CRA II to lead site monitoring and site management for clinical studies. You will ensure regulatory compliance, protect patient safety, and maintain study files, with travel as needed and potential
At Fortrea , we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist , you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory