fortrea

Fortrea Spain S.A. seeks a Site Regulatory & Contract Manager to lead country-level study start-up and regulatory submissions, ensuring trials activate on time and within budget.You will coordinate with Clinical Trial Coordinators, CRAs, regulatory, legal, finance and vendors, manage CTRAs and oversee quality, risk, and timelines across multiple studies in a...

The Site Regulatory & Contract ManagerThe Site Regulatory & Contract Manager is responsible for leading and overseeing country-level study start-up activities, ensuring clinical trials are initiated on time, within budget, and in compliance with applicable regulations and quality standards.Key ResponsibilitiesLead country-level regulatory submissions,...

Fortrea Spain is seeking a Senior Clinical Research Associate II (Sr CRA II) to lead site monitoring and site management for clinical studies in Madrid. You will ensure protocol adherence, regulatory compliance, and data integrity while coordinating with sponsors and Fortrea staff. The role requires extensive monitoring experience, strong knowledge of drug...

Job OverviewThe 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 II assures the implementation of project plans as assigned, functions as leader for projects of...

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 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 Senior Clinical Research Associate II (Sr CRA II) in Madrid to lead site monitoring activities for diverse clinical studies. You will ensure adherence to regulatory guidelines, manage monitoring plans, and liaise with investigators and vendors. The role requires 5+ years of clinical monitoring experience, strong data integrity focus, and...

Fortrea is seeking a CRA II with General Medicine expertise to join the FSP team in Spain. The role is permanent and involves site visits, regulatory compliance, and data quality oversight across studies. You will monitor sites, ensure patient safety, support regulatory submissions, and mentor junior staff while traveling as required. Fluency in Spanish and...

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 II assures the implementation of project plans as assigned, functions as leader for projects of limited...

Fortrea is seeking a CRA II with General Medicine expertise to join the FSP team in Spain. The role is permanent and involves site visits, regulatory compliance, and data quality oversight across studies. You will monitor sites, ensure patient safety, support regulatory submissions, and mentor junior staff while traveling as required. Fluency in Spanish and...

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...

Fortrea in Barcelona is seeking two CRA2 professionals to join our FSP team to monitor complex clinical trials in Gynecologic Oncology or Onco-Hematology. Descubra más sobre las tareas diarias, las responsabilidades generales y la experiencia requerida para esta oportunidad desplazándose hacia abajo ahora. The role includes site monitoring, ensuring...

Fortrea is seeking a CRA II with General Medicine expertise to join the FSP team in Spain. La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación. The role is permanent and involves site visits, regulatory compliance, and data quality oversight across...

Fortrea is seeking a Senior Clinical Research Associate II (Sr CRA II) in Madrid to lead site monitoring activities for diverse clinical studies. Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. You will ensure adherence to regulatory guidelines, manage monitoring plans, and liaise with investigators...

Fortrea is seeking a Site Start-Up Specialist to coordinate site activation, manage essential documents, and ensure timely regulatory submissions. Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud. You will work with the FSPx team and regulatory authorities to accelerate clinical trials. The ideal candidate...

Fortrea's FSP team is currently seeking a CRA II professionals to join the team in Galicia with specific experience in General Medicine, this is a permanent role.Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.Summary of Responsibilities:Clinical site...

Fortrea's FSP team is currently seeking two CRA II professionals to join the team in Galicia. Responsibilities * Clinical site monitoring: conducts routine, pre-study, initiation, and close-out visits, ensuring full compliance with project plans. * Site and patient protection: ensures informed consent, protocol adherence, and regulatory compliance to...

Fortrea's FSP team is currently seeking a CRA II professionals to join the team in Galicia with specific experience in General Medicine, this is a permanent role. Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud. Summary of Responsibilities: * Clinical site...

Fortrea Spain S.A.Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.seeks a Site Regulatory & Contract Manager to lead country-level study start-up and regulatory submissions, ensuring trials activate on time and within budget.You will coordinate with...