fortrea

Join Our Team and Drive Clinical Research Success! 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 submissions are completed efficiently. Your expertise...

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 critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical...

Fortrea's FSP team is currently seeking two CRA2 professionals to join the team in Barcelona. Candidates must have at least 3 - 4 years of experience working on complex clinical trials, specifically within Gynecologic Oncology or Onco - Hematology .Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring...

Fortrea is looking for a Site Budget & Contract Specialist to join its team in Madrid, Spain. In this role, you will be integral in negotiating site agreements and managing budgets to support clinical research efforts.You will collaborate with various departments and leverage industry tools to enhance processes and ensure compliance with regulations. Ideal...

Join Our Team and Drive Clinical Research Success! 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 submissions are completed efficiently. Your expertise...

Fortrea in Barcelona is seeking two CRA2 professionals to join our FSP team to monitor complex clinical trials in Gynecologic Oncology or Onco-Hematology. The role includes site monitoring, ensuring patient safety, data integrity, and adherence to regulatory requirements. Will liaise with vendors, coordinate visits, and support regulatory submissions. Travel...

Fortrea is seeking a Site Start-Up Specialist to coordinate site activation, manage essential documents, and ensure timely regulatory submissions. You will work with the FSPx team and regulatory authorities to accelerate clinical trials. The ideal candidate will have a life sciences background, 2+ years in clinical research, and strong organizational and...

Job Overview: The Clinical Trial Coordinator is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project.Summary of ResponsibilitiesDocument and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support.Assist in the preparation of study and...

Fortrea is seeking a Clinical Trial Coordinator in Madrid to support Clinical Project Teams with trial activities, documentation and TMF management.Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad.You will assist in preparing study materials, take minutes for sponsor meetings, and...

Fortrea is looking for a Site Budget & Contract Specialist to join its team in Madrid, Spain. In this role, you will be integral in negotiating site agreements and managing budgets to support clinical research efforts.You will collaborate with various departments and leverage industry tools to enhance processes and ensure compliance with regulations. Ideal...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Fortrea's FSP team is currently seeking two CRA2 professionals to join the team in Barcelona.¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación.Candidates must have at least 3 - 4 years of experience working on complex clinical trials, specifically within Oncology Gynecology / Hematology / Breast...

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 ResponsibilitiesResponsible for all aspects of study site monitoring including routine monitoring and closeout of clinical...

Summary of Responsibilities Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according to Fortrea's Standard...

Fortrea Spain is seeking an experienced Clinical Monitor to manage site activities for immunology trials, ensuring adherence to ICH GCP, SOPs, and sponsor requirements. You will oversee training verification, source data verification, and regulatory documentation while coordinating with the study team.The role requires 3–4 years of monitoring experience,...

Fortrea is seeking a Site Monitor to oversee clinical study monitoring and site management in Madrid. You will conduct routine visits, ensure protocol and regulatory compliance, and manage study files across sponsored trials, with travel as an essential function.Requirements include a university degree or equivalent allied health certification, ICH-GCP...

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 critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical...

Fortrea in Barcelona is seeking two CRA2 professionals to join our FSP team to monitor complex clinical trials in Gynecologic Oncology or Onco-Hematology. The role includes site monitoring, ensuring patient safety, data integrity, and adherence to regulatory requirements.Will liaise with vendors, coordinate visits, and support regulatory submissions. Travel...

Fortrea Spain is seeking an experienced Clinical Monitor to manage site activities for immunology trials, ensuring adherence to ICH GCP, SOPs, and sponsor requirements. You will oversee training verification, source data verification, and regulatory documentation while coordinating with the study team. The role requires 3–4 years of monitoring...

Summary of Responsibilities Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according to Fortrea's Standard...