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Research Nurse (Rn Or Lpn) / Madison, Wi (On-Site)

0-1 years
Not Disclosed
10 Oct. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Research Nurse (RN or LPN) / Madison, WI (On-Site)

Location: Madison, WI
Category: Patient Services
Job ID: 254229
Work Type: Full-time (On-Site)
Shifts Available: Multiple Night Shifts

  • 🕕 Weekdays (12-Hour Shift): 6:00 PM – 6:00 AM

  • 🌙 Weekdays (8-Hour Shift): 11:00 PM – 7:00 AM

  • 🌃 Weekends (12-Hour Shift): 6:00 PM – 6:00 AM
    Perk: Free on-site parking just steps away from the clinic 🚗


About the Organization

As one of the largest Clinical Research Organizations (CROs) globally, we operate four Early Phase Clinical Research Units across the UK and US.
We collaborate with leading pharmaceutical, biotechnology, and medical device companies, focusing on Phase I clinical development to establish the safety, tolerability, and pharmacokinetics of new investigational drugs.

Joining our team gives you the opportunity to:

  • Engage directly with healthy volunteer participants

  • Gain exposure to diverse study types (ascending dose, first-in-human, food effect, drug-drug interactions, etc.)

  • Be part of cutting-edge research that impacts patient lives worldwide


Position Overview

We are seeking Registered Nurses (RNs), Licensed Practical Nurses (LPNs), and Certified Paramedics to join our Early Phase Clinical Research Unit in Madison, WI.

You will:

  • Work in a fast-paced, team-oriented clinical setting

  • Maintain direct participant interaction

  • Practice and expand your clinical skills

  • Contribute to advancing medical innovation


Key Responsibilities

  • Utilize clinical skills and judgment to deliver a high standard of research-based care

  • Perform accurate vital sign measurements (blood pressure, pulse, respiration, temperature, weight)

  • Conduct venipuncture and ECG/Holter recordings

  • Collect and process biological samples per study protocol

  • Monitor participant dietary compliance

  • Assist in room preparation and medical equipment setup

  • Support screening procedures and study preparation

  • Maintain a clean, safe, and compliant work environment

  • Complete documentation accurately and promptly in electronic systems

  • Execute additional tasks as assigned to support study operations


Qualifications

Education

  • High School Diploma or equivalent (Required)

  • Additional clinical education preferred (RN/LPN/Paramedic)

Certifications (Preferred)

  • EMT, Phlebotomy, CMA, or CNA Certification

  • Paramedics must hold current certification

Experience

  • 0–1 year of related experience in a clinical or healthcare environment

  • New graduates and early-career professionals encouraged to apply


Ideal Candidate Profile

You thrive in an environment that is:

  • Fast-Paced: Precision and timing are critical—no room for protocol deviations

  • 🔄 Dynamic: Constantly shifting priorities require adaptability

  • 🤝 Team-Oriented: Collaboration and communication ensure study success

  • 💻 Tech-Driven: Comfortable with electronic data capture (EDC) and digital workflows


Work Environment

  • On-site clinical/laboratory setting

  • Exposure to biological samples and medical equipment

  • Electronic data collection systems utilized throughout


Compensation & Benefits

Regular full-time or part-time employees (20+ hours/week) are eligible for:

  • 🏥 Medical, Dental, Vision, Life, STD/LTD Insurance (multiple carriers)

  • 💰 401(k) Retirement Plan

  • 🏖️ Paid Time Off (PTO)

  • 🏆 Employee Recognition Awards

  • 🌍 Employee Resource Groups (ERGs)


Why Join Us

  • Gain hands-on exposure to Phase I clinical trials

  • Work with innovative therapies and emerging medical technologies

  • Contribute directly to advancing global healthcare

  • Enjoy career development, mentorship, and continuous learning


Equal Opportunity Statement

We are proud to be an Equal Opportunity Employer (EEO).
Learn more or request accommodations via our EEO & Accommodations page.