fortrea

The Senior Medical Coding Specialist will work within a sponsor-dedicated model, partnering closely with sponsor stakeholders and cross-functional clinical data management teams to provide medical coding expertise, oversight, and quality review across clinical development studies. This role serves a

The role Fortrea 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 days a week with the rest of the time being spent working from home. Ideally you will have at least

Fortrea is recruiting! Our FSP department in Paris is looking for a Senior Clinical Research Associate II (SCRA II). Key Responsibilities: Monitor Clinical Trials - conduct site visits to ensure compliance with protocols, regulatory requirements and Good Clinical Practice (GCP) - National on sites v

Are you looking to apply your analytical and technical skills to work that has a real impact on patients' lives? As a Statistical Programmer 1 at Fortrea, you will be part of a global team responsible for transforming clinical trial data into high-quality datasets and reports that support critical d

Job Overview: Directs territory sales strategy and execution, collaborating with senior leadership to shape account plans, optimize territory performance, and drive revenue growth. Leads, develops, and coaches Business Development Directors while fostering strong client relationships, identifying ne

Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate (CRA I or CRA II level) , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global e

Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA). This role offers the opportunity to monitor sites in Austria and in Switzerland, while working on cutting-edge studies that shape the future of healthcare. Key Responsibilities

Senior Medical Director US Remote Based Fortrea is seeking a Senior Medical Director to provide medical direction for the conduct of clinical trials. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring assig

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 Responsibilities: • Document and track study activities using relevant forms and tools, as well as relevant Project Management Syste

Are you passionate about developing people, driving operational excellence, and shaping the future of clinical research? We are looking for a Manager II, Clinical Operations to lead a team of clinical research professionals across the UK/IRE. This is an exciting opportunity to play a key leadership

Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adv

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 device customers a wide range of clinical development and technology solutions across more than 20

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 invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know wh

Fortrea - People with Disabilities (PwD) Talent Pool Fortrea is committed to building a diverse and inclusive workforce where everyone feels valued and has the opportunity to thrive. We believe that a variety of perspectives and experiences makes us stronger and enables us to better serve our custom

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before mo

Job Overview: The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially through closeou

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 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 aspects of

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 fo

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 Specialist, you will play a critical role in the clinical trials budgeting process. Your work will help drive the su