Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Research Nurse / Open To Rn's, Lpn's, Or Paramedics

Fortrea
Fortrea
0-1 years
Not Disclosed
Madison, United States
10 Feb. 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Research Nurse (RN, LPN, or Paramedic) – On-Site 

Location: Madison, Wisconsin
Job Category: Clinical Research / Patient Services
Employment Type: Full-Time (On-Site)
Experience Required: 0–1 year of related clinical experience

About the Organization

Join Fortrea, a leading global Contract Research Organization (CRO) delivering clinical development and technology solutions across more than 20 therapeutic areas. Operating in approximately 100 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-changing therapies.

With four Early Phase Clinical Research Units across the UK and the US, Fortrea plays a critical role in Phase I clinical trials—establishing the safety, tolerability, and pharmacokinetics of investigational treatments before they advance to later-stage development.

Role Overview

We are seeking Clinical Research Nurses, Licensed Practical Nurses (LPNs), and certified Paramedics to join our on-site Early Phase unit in Madison, WI. This position is ideal for healthcare professionals who are passionate about patient care and interested in transitioning into clinical research.

In this role, you will work directly with healthy volunteer participants in a fast-paced, protocol-driven environment. You will gain exposure to diverse therapeutic areas and study types, including first-in-human trials, ascending dose studies, food effect studies, and drug-to-drug interaction research.

This opportunity offers hands-on involvement in early drug development while maintaining meaningful, face-to-face participant interaction.

Key Responsibilities

  • Deliver high-quality clinical care in accordance with study protocols and regulatory standards

  • Perform vital sign assessments including blood pressure, pulse, respiratory rate, temperature, and weight

  • Conduct venipuncture and biological sample collection, processing, and protocol-specific distribution

  • Prepare and accurately record ECGs and Holter monitor readings

  • Monitor participant dietary compliance during study periods

  • Support screening procedures and participant evaluations

  • Prepare clinical rooms and ensure proper setup of medical equipment

  • Maintain a clean, organized, and audit-ready clinical research environment

  • Accurately document study data within electronic data capture systems

  • Collaborate cross-functionally to ensure adherence to timelines and protocol requirements

Required Qualifications

  • High School Diploma or equivalent

  • Active RN or LPN license, or certified Paramedic (Paramedics must hold Wisconsin state certification)

  • 0–1 year of related clinical or healthcare experience

  • Strong attention to detail and ability to follow strict protocols

  • Comfort working in a technology-driven, electronic documentation environment

Preferred Qualifications

  • EMT, Phlebotomy, CMA, or CNA certification

  • Prior exposure to clinical research or early phase studies

Work Environment Expectations

  • Fast-paced, compliance-focused setting with zero tolerance for protocol deviations

  • Frequently shifting priorities requiring adaptability and time management

  • High level of teamwork and communication

  • Fully electronic clinical data systems

Compensation and Benefits

Employees working 20 or more hours per week are eligible for comprehensive benefits, including:

  • Medical, Dental, and Vision Insurance

  • Life Insurance and Short-Term/Long-Term Disability coverage

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Programs

  • Employee Resource Groups (ERGs)

  • On-site free parking

Physical Requirements

  • Ability to stand or remain upright for 6–8 hours per shift

  • Repetitive hand and wrist movements to operate clinical and laboratory equipment

  • Occasional bending, crouching, stooping, and upper body movement

  • Light to moderate lifting (up to 15–20 lbs)

  • Consistent and reliable attendance

  • Flexibility to work varied shifts as needed

Why Join Fortrea

At Fortrea, you will be part of a mission-driven organization committed to advancing clinical research and improving patient outcomes worldwide. Through its FOUR values—Forward Together, Own It, Uphold Integrity, and Respect People—the organization fosters professional development, collaboration, and innovation.

This position offers a strong foundation for healthcare professionals seeking to build a long-term career in clinical research while contributing directly to the development of future therapies.

Apply now through ThePharmaDaily.com to advance your clinical career in early phase research.