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 Costing Manager is a position that sits within the Costing Department, as part of the ECS group. The role is primarily charged with supporting the Costing Directors in the delivery of clinical study costings and
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, record, and report Adverse Drug Reaction in timelines (according to the
Job Overview: Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US, EU, Japan, and ROW health authorities and oversight of the same, as applicable. Summary of Responsibilities: These statements are intended to describe the
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Job Overview: Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of
Position Overview The Accounting Senior Associate will play a key role in supporting the monthly and quarterly consolidated close process, ensuring timely, accurate, and well-controlled financial reporting deliverables. This role requires a highly analytical accounting professional
Fortreas FSP team is hiring a Clinical Operations Manager- Regulatory - Hybrid in Montreal, Canada. Must be bilingual in French & English. Candidates with strong organizational skills, attention to details, and the ability to manage financial processes
Fortreas FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal, Canada. Must be bilingual in French & English. Candidates with strong organizational skills, attention to details, and the ability to manage financial processes
Senior Clinical Programmer Analyst Remote | Mexico Join Fortrea and work from anywhere in Mexico while contributing to global clinical trials that help bring life-changing therapies to patients worldwide. Were seeking an experienced Senior Clinical Programming &
Job Overview: The Clinical Trial Manager II has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Job Overview: Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
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 I, you will play a pivotal role in coordinating site start-up
Job Overview: The Clinical Trial Manager I has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities
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
Our FSP team is currently seeking a CRA 2 in West Region with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will
Job Overview: Do you have proven experience working as a project/financial analyst within a Contract Research Organization (CRO) or pharmaceutical company providing financial insight on international clinical trials? Do you have a natural ability to communicate
Are you an experienced contracts professional looking to take the next step in your clinical research career? Join us as a Contract Specialist II and play a key role in negotiating and executing clinical trial agreements
Senior Coding Specialist Costa Rica Candidates must be based in Costa Rica Are you passionate about medical coding quality and clinical data integrity? We’re looking for a Senior Coding Specialist based in Costa Rica to support