fortrea

Company Overview: 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, patient access, and techno

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 skills, knowledge, and clinical judgement to provide a high standard of care for partic

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

Our CPS team is currently seeking a Study Start Up Specialist with 2+ years of start-up experience residing with the U.S. Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essen

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Clinical Research Technician to interact directly with our healthy volunteer participants while learning to read clinical research protoco

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

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

Job Overview: Assist in the development and implementation of solutions to DM service issues and concerns regarding Medidata RAVE, Oracle Inform, CRF Design, and Data Capture or imaging activities, including proactive prevention strategies. Develop and maintain programs for creation of datasets as p

We are currently seeking a RWE Programmer to join a sponsor-dedicated team supporting a global pharmaceutical partner. This is a fully home-based opportunity. As a RWE Programmer, you will serve as a subject matter expert in Real World Data analytics and support the analysis of large healthcare data

We are seeking a detail-oriented and commercially minded Contract Specialist to support project budgets, as well as the preparation, review, negotiation, and execution of a variety of client contracts within the pharmaceutical and CRO industry. This role partners closely with Legal, Finance, Strateg

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: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience, and level of contribution which they can make to the proj

Job Overview: The Executive Director, Business Development is a strategic business partner who leads a team of Business Development Directors at all levels to develop and expand new business opportunities while growing and maintaining existing accounts. The role steers overall growth initiatives, se

****This role is within a processing lab and not an analytical lab.**** As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Lab Technician to interact directly with our healthy volunteer par

Job Overview: Provide foundational operational support to the supplier qualification lifecycle, ensuring accurate documentation and compliance with procedures. Summary of Responsibilities: Support defined steps of the supplier qualification and re‑qualification processes. Accurately collects, organi

Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking an Clinical Research Coordinator, to interact directly with our healthy volunteer participants while learning to read clinical research prot

Fortrea is hiring a Vice President, Therapeutic Area Leader focused on oncology to provide global scientific, strategic, and operational leadership within this assigned Therapeutic Area. This role shapes and executes the global medical strategy within the oncology team / therapeutic area in alignmen

Clinical Research Registered Nurse - Early Phase Clinical Trials (Multiple Shifts Available) Location: Daytona Beach, FL Schedule Options: Option 1: Rotating Shift 10-hour shifts Rotating weekends to include a 12-hour shift Option 2: Mid Shift 10-hour shifts Start time between 11am and 1pm Rotating

The Executive Director, Project Management (RWE & Phase IV Studies) leads a global team of project management professionals and is accountable for the operational delivery, financial performance, quality outcomes, and client satisfaction of the RWE and Phase IV project management portfolio. Reportin