Fortrea
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About the Company
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
Open Positions
57Job Overview:Leads validation projects as assigned and serve as a validation team member on multiple assignments as designated by the management with support from other team members as needed. Serve a...
The roleFortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London.This client-dedicated role is to be office based in central London for at least 3 da...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regul...
The Marketing Senior Manager for the Therapy Area Marketing supports the development and execution of therapy‑specific marketing strategies that advance business priorities and customer engagement. Th...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regul...
Job Overview:This role will exhibit strong leadership, maintain a keen focus on future growth opportunities and industry trends, and position the organization to adapt to market shifts and maintain a ...
Summary of Responsibilities:Coordinates and oversees Regulatory Authority, Ethics Committee/Institutional Review Board, Third Body submissions for all study types across multiple countries globally in...
Fortrea's FSP team is hiring a Manager, Site Agreements!Home Based in USA and able to work EST hours.Must have 5+ years of investigator budget and contract negotiation experience working with CROs and...
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 impleme...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regul...
Providing full support to the Flexible Solutions group to facilitate client delivery by e.g.· Support in tracking of compliance KPIs/metrics, root causes and mitigations· Support in tracking informati...
This role plays a key part in supporting Fortrea’s end‑to‑end proposal development process for RFPs, RFIs and client budget requests. You will coordinate and prepare high‑quality proposal deliverables...
Full time. Remote in the UK, Spain, Portugal or Greece.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we can´t do it alone. We are seeking an exper...
Job Overview:It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. The individual...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regul...
Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regul...
Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.Receive information, recor...
Job Overview:The Centralized Study Specialist II is a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Centraliz...
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 impleme...
Fortrea is seeking an Associate Project Finance Associate to join our Project Finance Management team. This entry-level role is ideal for early-career professionals looking to grow their financial acu...
Job Overview:The Centralized Study Specialist II is a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Centraliz...
Fortrea is currently seeking a US remote based Sr Specialist, Clinical Data Strategy & Operations (CDSO) – FSP to drive and support process development, evaluation, and implementations projects that a...
Job Overview:Support site(s) by providing guidance and EHS knowledge to help minimize employee illness and injuries. Assist in ensuring compliance with regulatory requirements and relevant industry st...
Fortrea is currently seeking a US remote based Associate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical kno...
Our FSP Team is hiring SSU Specialists! Remote in the US!Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of t...
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requireme...
Job Overview:Responsible for creation/revision/compilation/approval of Documents for submission by Fortrea clients to US, EU, Japan, and ROW health authorities and oversight of the same, as applicable...
Apprentice – IT Project ManagementAbout the teamWe are seeking a savvy, motivated IT Project Management Apprentice to join our team. This will provide you with an unforgettable experience in a dynamic...
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Screening Technician, to interact dire...
Summary of Responsibilities:Follow applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Administer controlled documen...
Summary of Responsibilities:Coordinates and oversees Regulatory Authority, Ethics Committee/Institutional Review Board, Third Body submissions for all study types across multiple countries globally in...
This individual will leverage advanced analytics and data science techniques to support the Commercial Sales organization through actionable insights, predictive modeling, and data-driven strategies. ...
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requireme...
Job Overview:The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job.Summar...
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Research Nurse (RN's, LPN's), to intera...
This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invit...
Job Overview:Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period.Summary of Responsibilities:Undertake prim...
Job Overview:Minimum 2–3-year experience in a similar job in pharmaceutical companies, international CRO or providers of clinical digital servicesReports directly to the FSP Fortrea Line Manager.Recei...
We are currently seeking Experienced Ophthalmology CRA 1 to complete our FSO team. WHAT YOU WILL DOYou will utilize your skills, knowledge, and clinical judgement to provide a high standard of care fo...
Summary of Responsibilities:Investigator Payments:Review EDC, Contract, and process payments in payment system.Work with PA to generate cover letter or Proforma invoice and payment batch generation in...
Job Overview:Minimum 8-year experience in epidemiology, pharmacoepidemiology, non-interventional studies (prospective studies, patient registries, retrospective database studies), RWE generation in bi...
Love writing. Thrive on deadlines. Interested in clinical research?We’re hiring an RFI Associate to support global business development opportunities in a fast‑paced CRO environment. You’ll help manag...
Job DescriptionFortrea's FSP team is hiring experienced Sr. Project Managers! Seeking current Sr. PMs with recent experience working for a Sponsor directly or within a FSP model. Oncology experience r...
Lead Teams. Elevate Operations. Drive Start‑Up Excellence.We’re looking for an inspiring Clinical Operations Manager to lead a team of 20 professionals across clinical operations — ensuring excellence...
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 impleme...
Location: Fully remote, based anywhere in ROIEmployment Type: Full-time, Client-Dedicated We are seeking a Regulatory Study Start-Up Project Manager to join our team. In this role, you will work 100% ...
Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical research. In this position, you will support the execution of clinical studies that contribute to impr...
Job Overview:Responsible for preparation and coordination of clinical study protocols and clinical study reports (CSRs), and other documents as needed. Provide support for and participate in developme...
Summary of Responsibilities:Develop and review contracts for low to medium complexity projects and see through to execution (including MSAs, CDAs, ISAs, IPAs, WSCs, budgets if required, etc.) – up to ...
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 Specia...
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requireme...
Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development.The TMF Management team is responsible for the completeness and accuracy...
Be the connection between science and solutions. In this CRA position, you’ll help transform complex clinical protocols into real-world results, working alongside a team that values precision, integri...
Job Overview:Lead the preparation and review of aggregate safety, risk management, signal detection, and benefit-risk evaluation reports. Be responsible for end-to-end report management, including pla...
Summary of Responsibilities:To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc.Receive information, recor...
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical...
The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations, including financial entities support...