fortrea

Job Overview:The Aggregate Report Specialist is responsible for supporting core pharmacovigilance deliverables, including scheduled and ad hoc aggregate reports, while ensuring high-quality, timely execution of assigned activities. The role involves collaboration with cross-functional stakeholders, quality review of reports, mentoring junior team members,...

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...

Fortrea in Madrid is seeking a site monitor with clinical trial experience to oversee site activities, ensure protocol compliance, and protect patient safety. The role includes pre-study visits, vendor liaison, and data integrity checks, with travel as needed.The candidate should have a university degree and at least six months in a related role, strong...

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...

Job OverviewAt 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 will help bring life-changing treatments...

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...

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 study site monitoring including routine monitoring and closeout of...

Fortrea seeks an Aggregate Report Specialist to support pharmacovigilance deliverables such as PBRERs, PADERs, and line listings. You will coordinate reporting activities, perform data analysis, and ensure timely quality reviews across cross-functional teams. You’ll mentor junior staff, monitor timelines, contribute to process improvements, and participate...

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 study site monitoring including routine monitoring and closeout of...

Job OverviewAt 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 will help bring life-changing treatments...

Fortrea is seeking a Site Budget & Contract Specialist to negotiate and manage site agreements, confidentiality agreements, and related contracts for clinical trials. You will support regulatory compliance, maintain contract status, and collaborate with study teams to ensure timely execution. Joining the FSPx team, you will work with key sponsor projects to...

Fortrea is seeking a Site Start-Up Specialist in Madrid, Spain, to coordinate site activation, manage essential regulatory documents, and ensure timely submissions in line with ICH/GCP guidelines. You will work within the FSPx team, collaborating with sponsors and clinical teams to advance trials. The role requires a life sciences-related degree or allied...

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...

Fortrea is seeking a Site Start-Up Specialist to coordinate site activation and regulatory submissions. You will manage essential documents, ensure ICH/GCP compliance, and submit country-specific forms with accuracy.The role involves collaboration with internal teams and external stakeholders, including regulatory authorities, to maintain audit-ready...

Fortrea is seeking a dedicated Europe remote based Medical Director or Senior Medical Director with deep expertise in Ophthalmology, including cell and gene therapies. The role provides medical leadership across all development phases and medical monitoring for assigned studies. The successful candidate will lead ophthalmology clinical programs, engage with...

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....

Fortrea is seeking a Delivery Director - Immunology & Respiratory Expertise to lead the Clinical Delivery CoE portfolio, ensuring on-time, on-budget delivery and high quality across studies. The role requires extensive leadership, client relationship development, and cross-functional collaboration to drive financial performance and operational excellence in...

Job OverviewAt 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 will help bring life-changing treatments...

Fortrea in Barcelona is seeking a Site Monitor to manage clinical studies on site, ensuring adherence to ICH GCP, SOPs and regulatory guidelines with a strong focus on data integrity and trial conduct. The role requires a university degree, fluent Spanish and English, and at least two years as an independent monitor. Oncology trial experience is highly...

Fortrea is seeking a Study Start-Up Lead to drive planning and activation of clinical trials on a sponsor-dedicated team. You will mentor SSU teams, develop forecasting models, and ensure ICFs meet local requirements for global programs. The role emphasizes data-driven decision-making, process improvement, and collaboration with Clinical Operations to...