fortrea

Job Overview The Clinical Trial Coordinator (CTC) serves as a key liaison between investigative sites, sponsors, vendors, and internal study teams, supporting financial and operational activities throughout the clinical trial lifecycle. This role is responsible for coordinating site payments, budget

Job Overview: Manage ‘Client’ or ‘Project’ specific 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) for specified projects. Manage and process e

At Fortrea, your career is more than just a job – it's a journey of innovation, impact, and purpose. Every day, you’ll help advance life-saving therapies and transform the lives of patients around the globe. Together, exceptional is possible. We are currently proactively engaging with talented CRAs

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 DM activities (from study start-up to data

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 regulations and to internal WI/

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 regulations and to internal WI/

Job Overview: Responsible for preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices. Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. Assist Medical Write

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

We are on a mission to discover new treatment answers for patients in times of need. But we can´t do it alone. We´re seeking an experienced Pricing & Data Analyst to optimize our pricing strategies, directly impacting the financial grow for our Clinical Pharmacology Services (CPS). This is why we ne

Do you have a passion for scientific writing and clinical research? Then, join Fortrea as our next Medical Writer 1 and help ensure new medicines are safe for patients while kick-starting a global career in clinical trials. Fortrea Clinical Pharmacology Services (CPS) supports the earliest and most

Senior Clinical Data Manager – sponsor dedicated Joining Fortrea’s Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from across th

Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in Oncology. In this role, you will ensure the successful execution of clinical studies on a local level, while maintaining high-quality standards and regulatory compliance. This role is for upcoming future opportu

Job Overview: Global HR Business Partner and primary HR advisor to senior functional leaders and/or direct reports to C-suite executives supporting complex global functions and organizations. Member of respective leadership teams. Active participant in the development of business and functional stra

Experienced EU-based Respiratory Project Managers. We are looking for Project Managers and Senior Project Managers with: Strong respiratory therapeutic expertise, ideally including asthma, COPD, ILD, severe respiratory disease, pulmonary fibrosis, or related indications. Experience leading global Ph

12-Month University Student Placement – Statistical Programming – Leeds (Office-Based) – Start Date July 2027 At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship – it’s a launchpad for your future. As a Statistical Programming Inte

Job Description At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship, —it’s a launchpad for your future. As an Intern, you’ll join a global team where curiosity, motivation, and fresh ideas are celebrated. You’ll work on meaningful

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency

Job Overview: The mission of the Project Management Academy (PM Academy) is to identify and develop potential clinical project management leaders of the future. Within a face-to-face, continuous learning environment, Project Coordinators (PC) are the right-hand support to the Project Lead. The Proje

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 of contact for investigative sites, this role ensur