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

Position: Clinical Research Nurse (Open to RN’s, LPN’s, or Paramedics)

Location: Madison, WI (On-Site)
Category: Patient Services
Job ID: 254235


🌟 Highlights

  • Free Parking Onsite 🚗

  • Employment Type: Full-Time (Office/Clinic-Based)

  • Location: Madison, Wisconsin


🏢 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.

You’ll be part of a team working alongside world-leading pharmaceutical, biotechnology, and medical device companies during the earliest phase of drug development, focusing on evaluating the safety, tolerability, and pharmacokinetics of new drugs.

This is an ideal role if you’re seeking:

  • Direct interaction with healthy volunteer participants

  • A dynamic, fast-paced, team-oriented clinical research environment

  • Exposure to a variety of therapeutic indications and study types, including:

    • Ascending Dose Studies

    • First-in-Human Trials

    • Food Effect Studies

    • Drug-to-Drug Interaction Studies


💊 Role Overview

In this role, you’ll combine your clinical judgment, technical expertise, and patient care skills to deliver high-quality service within a Phase I research setting.

You’ll maintain face-to-face engagement with participants, apply your clinical knowledge, and work with the latest medical technologies and treatments, contributing directly to life-changing drug development.

💡 When a drug you’ve worked on reaches approval, you’ll know your contribution has helped improve countless lives globally.


🩺 Key Responsibilities

  • Deliver a high standard of clinical care using nursing knowledge and judgment

  • Perform and document:

    • Vital signs (BP, pulse, respiration rate, temperature, weight)

    • Venipuncture and blood draws

    • ECG/Holter preparation and recording

  • Collect and process biological samples as per protocol, ensuring accurate labeling and distribution

  • Monitor meals to ensure participant dietary compliance

  • Prepare rooms and medical equipment for study use

  • Assist with participant screening procedures

  • Maintain a clean, organized, and safe clinical environment

  • Perform other assigned duties to support study success


🎓 Qualifications

Education:

  • Required: High School Diploma or equivalent

Preferred Certifications:

  • EMT, Phlebotomy, CMA, or CNA

Experience:

  • 0–1 year of related clinical experience

  • Paramedics: Must hold state certification (Wisconsin)


Work Environment

This role is ideal for individuals who thrive in settings that are:

  • Fast-Paced: Timeliness is critical — even small delays can impact study quality

  • Dynamic: Priorities may shift frequently; adaptability is essential

  • Collaborative: Strong teamwork and communication are key to success

  • Technology-Driven: Data collection occurs directly in electronic systems


💎 Benefits

Employees working 20+ hours per week enjoy a comprehensive benefits package, including:

  • Medical, Dental, Vision Insurance (Multiple Carriers)

  • Life Insurance

  • Short- and Long-Term Disability (STD/LTD)

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Awards

  • Employee Resource Groups (ERGs)


📋 Additional Information

To learn more about Equal Employment Opportunity (EEO) policies and accommodation requests, please refer to our official EEO documentation.