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Senior Medical Director, Rheumatology - US Remote Based Fortrea is looking for a Senior Medical Director, Rheumatology (Remote, US-Based) to play a pivotal role in the development of innovative therapies for autoimmune…
Our Phase I team is currently seeking a Senior Clinical Research Associate with 3+ years of experience. Ideal candidates would have phase I experience and reside in the U.S. WHAT YOU WILL DO You will utilize your…
Summary of Responsibilities: Duties include diverse coordination and administrative tasks and activities. May organize multiple processes, procedures, or programs. Responsible for reviewing and supporting the logistics…
Our FSP team is seeking Project Managers/Sr. Project Managers t o j oin our growing team. This role requires 2-5 + years of global project management experience , with experience in Oncology or Ophthalmology .…
Job Overview: The aCRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country…
Job Overview The Executive Director Epidemiologist within Fortrea Consulting is a senior leader for the epidemiology capability. The role provides scientific governance for the most complex or high-risk epidemiology…
Fortrea's FSP team is currently seeking two CRA2 professionals to join the team in Barcelona. Candidates must have at least 3 - 4 years of experience working on complex clinical trials, specifically within…
We’re excited to announce a new opportunity to join our growing team in Australia! We are currently seeking a Clinical Research Associate II (CRA2) who is passionate about advancing clinical research and making a…
The Site Regulatory & Contract Manager is responsible for leading and overseeing country-level study start-up activities, ensuring clinical trials are initiated on time, within budget, and in compliance with…
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…
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…
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…
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. As a Clinical Research Technician II you will perform practical / administrative…
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…
Summary of Responsibilities: Based on forecast models, manage the resources to meet or exceed business Service Level Agreements. Supervise, Mentor, Evaluate and aid in staff development, career development, people…
Come join Fortrea today as a part-time Nurse Practitioner with our Phase I site based in Madison, Wisconsin. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the…
Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing in the West Coast region. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high…
Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance…
Main Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including…
Role Overview We are seeking a detail-oriented and research-savvy librarian to support our pharmacovigilance team by conducting systematic literature searches to identify safety signals, adverse drug reactions (ADRs),…
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