We are currently seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. CAR-T desired. Open to major hub locations across the
We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. Open to major hub locations across
Join Fortrea as a Senior Clinical Research Associate II in Türkiye within a sponsor-dedicated model, where you will work exclusively with a leading global biopharmaceutical partner. In this role, you will support the delivery of high-quality clinical
Are you passionate about clinical trial budgeting, financial strategy, and delivering accurate, competitive study cost estimates? Join Fortrea as an Investigator Grants Manager / Clinical Trial Costing Manager and play a critical role in shaping successful clinical
Job Overview: We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. This individual will take responsibility for the development of the project documentation, system set-up, data entry and
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 (location: Switzerland, Home-based), you will play a pivotal role in coordinating
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all
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 (location: Switzerland; Home-Based), you will
What if your project leadership skills helped new medicines take their first step in human clinical trials? Fortrea is one of the world´s largest and longest-established early-phase clinical research organizations. From first-in-human to exploratory biomarker or complex
What if your project leadership skills helped new medicines take their first step in human clinical trials? Fortrea is one of the world´s largest and longest-established early-phase clinical research organizations. From first-in-human to exploratory biomarker or complex
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
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
The Executive Director, Clinical Platforms & Product Development is a senior technology and operations leader responsible for defining, building, and operationalizing Fortrea’s Clinical Platforms ecosystem. This role serves as the strategic and operational partner to the Vice
Associate II, Patient Safety Solutions Remote Based in Canada Fortrea is currently seeking a remote based Associate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case processing. This role requires strong clinical
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) US Remote Fortrea is seeking a Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) is responsible for supporting and overseeing Clinical Safety and Pharmacovigilance Services (PSS) operations associated with safety data
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
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 manage RFIs end‑to‑end — reviewing requirements, pulling inputs from
Job Overview: The Director level of SDG is an experienced leader within Strategic Delivery and Growth (SDG), expected to leverage their Research and Development experience, Therapeutic Area (TA) experience and operational study execution experience to sustainably
Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As an unblinded Clinical Research Associate , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative
The RCM Billing Manager will be responsible for all processes and resources related to billing procedures, including project / contract setup, invoicing, processing rebates, and processing credits and rebills, but not limited to the following: Summary