Nurse Practitioner (NP) - Onsite Madison, WI Phase I Site

FTCRUMAD Fortrea Clinical Research Unit Inc.

Alabama

On-site

USD 90,000 - 120,000

Full time

8 days ago
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Job summary

Fortrea Clinical Research Unit Inc. invites experienced Nurse Practitioners to join our Phase I site in Madison, Wisconsin. You will perform physical exams, take medical histories, and manage participant assessments under Medical Director guidance, while ensuring GCP compliance and regulatory liaison.

The role emphasizes clinical mentorship, cross-functional collaboration, and ongoing process improvements. The ideal candidate holds NP certification with active licensure, 3–5 years of clinical

Qualifications

  • Graduate of an accredited Nurse Practitioner program.
  • Current NP certification and active licensure.
  • 3–5 years of relevant clinical experience.

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.

Education

Nurse Practitioner program

Job description

Come join Fortrea today as a Nurse Practitioner with our Phase I site based in Madison, Wisconsin.

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.

At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

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