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What is Fortrea?

A Fortrea job typically refers to a position at Fortrea, a global contract research organization (CRO) that provides clinical trial management and drug development services. Employees at Fortrea work in various roles, including clinical research, data management, regulatory affairs, and project management, supporting pharmaceutical and biotech companies. These jobs involve conducting and overseeing clinical studies to ensure compliance with regulatory standards and accelerate the development of new treatments. Fortrea offers opportunities in diverse therapeutic areas and stages of clinical research, making it a key player in the life sciences industry.

What does Fortrea do?

Fortrea is a global contract research organization (CRO) that provides clinical development and research services to pharmaceutical, biotechnology, and medical device companies. The company specializes in conducting clinical trials, managing data, and supporting regulatory submissions to help bring new therapies and medical products to market. Fortrea's services include clinical trial design, patient recruitment, laboratory testing, and data analysis, making them an essential partner in the drug development process. Their work supports advancements in healthcare by ensuring new treatments are tested safely and efficiently.

What types of projects can I expect to work on as part of the Fortrea team, and how does the organization structure cross-functional collaboration?

As a member of the Fortrea team, you'll likely engage in a variety of clinical research projects, ranging from early-phase trials to late-stage studies for pharmaceutical and biotechnology clients. The work environment is highly collaborative, often involving cross-functional teams that include clinical research associates, project managers, data analysts, and regulatory specialists. Regular meetings and transparent communication channels support effective teamwork and project delivery. You'll have the opportunity to learn from experts across disciplines, which not only enhances project outcomes but also fosters your professional development and exposure to multiple facets of the clinical research process.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Fortrea, and why are they important?

To thrive as a Clinical Research Associate at Fortrea, you need a solid background in life sciences or a related field, relevant clinical research experience, and often a bachelor's degree or higher. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills for managing site relationships and regulatory compliance. These skills ensure the integrity, efficiency, and regulatory adherence of clinical trials, directly impacting patient safety and research outcomes.

What is the difference between Fortrea vs Clinical Research Associate?

AspectFortreaClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or RAC are commonRequires a degree in life sciences or healthcare; certifications like CCRA or RAC are often preferred
Work EnvironmentWorks primarily in clinical trial sites, offices, or remotely, supporting multiple projectsWorks at clinical trial sites, monitoring study progress and ensuring compliance
Employer & Industry UsageFortrea is a global contract research organization (CRO) providing clinical trial servicesClinical Research Associates are employed by CROs, pharmaceutical companies, or research institutions

While both roles involve clinical trial oversight, Fortrea is a CRO that employs Clinical Research Associates (CRAs) to manage and monitor clinical studies. CRAs focus on site visits and compliance, whereas Fortrea provides comprehensive trial management services across multiple projects and locations.

What kind of jobs does Fortrea offer?

Fortrea offers a range of jobs primarily in the clinical research and pharmaceutical sectors, including roles such as clinical research associates, project managers, data managers, and regulatory affairs specialists. These positions often require relevant scientific or healthcare backgrounds and may involve working in a team environment with specific industry certifications or training.

What are popular job titles related to Fortrea jobs in Wisconsin?

For Fortrea jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Fortrea jobs in Wisconsin look for?

The top searched job categories for Fortrea jobs in Wisconsin are:

Fortrea jobs near you
Infographic showing various Fortrea job openings in Wisconsin as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 42% Physical, 1% Hybrid, and 57% Remote job distribution.

Nurse Practitioner (NP) - Onsite Madison, WI

Fortrea

Madison, WI

Full-time

Posted 7 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 74 rated research

Job description

Come join Fortrea today as a 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 clinical aspects of trials conducted within Clinical Pharmacology. This role supports the execution of clinical studies and may function as a sub-investigator, ensuring high standards of participant safety, data integrity, and regulatory compliance.

Summary of Responsibilities

  • Perform physical examinations, medical histories, and participant assessments as delegated by the Medical Director

  • Interact with regulatory bodies as relevant to operational activities

  • Serve as a technical advisor to Clinical Pharmacology teams and cross-functional partners

  • Support the maintenance and continuous improvement of clinical processes and facilities

  • Participate in clinical feasibility assessments for new study proposals

  • Oversee and contribute to the development and implementation of quality systems to ensure adherence to Good Clinical Practice (GCP)

  • Ensure compliance with FDA, GCP, and ICH regulations

  • Perform routine study-related activities as required

  • Support sponsor visits and interactions in collaboration with operations and client management

  • Promote and maintain a safe working environment; recommend improvements as appropriate

  • Attend investigator meetings as needed

  • Serve as an educational resource, trainer, and mentor to staff

  • Perform additional duties as assigned

Qualifications (Minimum Required)

  • Graduate of an accredited Nurse Practitioner program

  • Current NP certification and active licensure

  • Equivalent combination of education and relevant experience may be considered

  • Strong English communication skills (spoken and written)

Experience (Minimum Required)

  • 3-5 years of relevant clinical experience

Physical Demands / Work Environment

  • Work is performed in a clinical and/or laboratory environment with potential exposure to biological, hazardous, or radioactive materials

  • Ability to distinguish colors and hear clearly

  • Ability to use hands for extended periods (up to 6 hours/day) for clinical and computer-based tasks

  • Ability to stand, walk, bend, and perform repetitive movements for extended periods (up to 6 hours/day)

  • Flexibility to work overtime or weekends as needed

Travel Requirements

  • Occasional travel may be required for investigator meetings, cross-site support, or training

Why Fortrea?

At Fortrea, you'll contribute to advancing clinical development and improving patient outcomes through meaningful work in early-phase research. This role offers a collaborative, fast-paced environment with opportunities to expand your clinical expertise and impact global healthcare innovation.

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