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Fortrea is a global clinical research organization serving biopharmaceutical and medical technology companies. Its clinical development services span clinical pharmacology, Phase I–IV study management, regulatory strategy, and market access, combining scientific expertise with data-driven approaches. Fortrea supports programs across areas including cell and gene therapy, oncology, cardiovascular disease, and infectious diseases, helping clients make informed development decisions and advance potential treatments toward patients.
Clinical Research Associate II - Fortrea Hybrid US
Monitor clinical trial sites across the US for Fortrea, supporting participant safety, protocol compliance, data quality, and adverse-event reporting.
United States
California
Colorado
Connecticut
Idaho
Illinois
Iowa
Kansas
Massachusetts
Michigan
Missouri
Montana
Nevada
New Jersey
New York
North Carolina
North Dakota
Ohio
Oklahoma
Oregon
Pennsylvania
South Carolina
South Dakota
Tennessee
Texas
Utah
Virginia
Washington
Wyoming$100,000 – $112,000 / year
HybridFull-timeJuniorMiddleEnglish RequiredClinical ResearchDescription
- Provide high-quality participant care during clinical trials and respond to emergencies according to research standards
- Monitor study sites through routine visits and close-out activities
- Maintain study documentation and conduct pre-study and initiation visits
- Coordinate with vendors and complete other assigned responsibilities
- Manage sites in line with project plans
- Provide study staff with the materials and guidance needed for safe patient enrollment
- Confirm that informed consent and protocol procedures meet applicable regulations
- Protect data integrity by reviewing source documents and case report forms
- Identify missing or implausible data
- Manage clinical trial registries and complete feasibility activities when requested
- Prepare and complete Serious Adverse Event reports, narratives, and follow-up
- Review CRFs independently and create or resolve queries in Fortrea or client data systems
- Support new-employee training through activities such as co-monitoring
- Coordinate assigned clinical projects as a Local Project Coordinator, with supervision when applicable
- Serve as a local client contact when assigned
Requirements
- Live near a major US hub airport
- Have two years of clinical monitoring experience
- Hold a university or college degree, or certification in a related allied health profession from an appropriately accredited institution, such as nursing licensure
- Be available for 60% overnight travel
- Work effectively in a fast-paced environment with strict adherence to study protocols
- Manage shifting priorities and adapt quickly
- Demonstrate teamwork and interpersonal skills
- Work in a technology-based environment and collect data electronically
- Sit for extended periods and operate a vehicle safely
- Perform repetitive hand, finger, and wrist movements quickly and repeatedly
- Occasionally crouch and stoop, with frequent bending and twisting of the upper body and neck
- Access and use varied in-house and commercial computer software
- Lift and carry light to moderate loads, including luggage and a laptop, weighing up to 15–20 lbs
- Maintain regular and consistent attendance
- Work varied hours when required
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