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Research Nurse Ii

Fortrea
Fortrea
2-3 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

Research Nurse II – Madison, WI (On-Site)

Location: Madison, Wisconsin, USA
Category: Patient Services
Job ID: 26371

About the Role
As a leading global Clinical Research Organization (CRO), we operate Early Phase Clinical Research Units across the US and UK, collaborating with top pharmaceutical, biotechnology, and medical device companies. We are seeking a Clinical Research Nurse II in Madison, WI, to provide direct care to healthy volunteer participants while gaining experience in clinical research protocols in a fast-paced, team-oriented environment.

This full-time, clinic-based role offers exposure to diverse therapeutic indications and study types, including ascending dose studies, first-in-human trials, food effect studies, and drug-drug interaction trials.

By joining us, you will play a critical role in early-phase clinical development, ensuring the safety, tolerability, and pharmacokinetics assessment of investigational drugs.

Key Responsibilities

  • Deliver high-quality clinical care using professional nursing judgment.

  • Accurately perform vital signs assessments, including blood pressure, pulse, respiratory rate, temperature, and weight.

  • Prepare and record ECGs/Holters with precision.

  • Collect, process, and appropriately distribute biological samples per protocol.

  • Monitor participant dietary compliance and ensure study adherence.

  • Assist in room and equipment preparation for clinical procedures.

  • Support screening procedures and other study-related activities.

  • Maintain a clean, safe, and compliant clinical environment.

  • Perform additional duties as assigned to support study success.

Requirements

  • Associate degree or Bachelor of Science in Nursing (BSN) with current state licensure.

  • CPR/AED certification required; ACLS certification preferred.

  • Minimum of 2–3 years of nursing experience; additional clinical experience may substitute for educational requirements.

  • Comfortable working in a fast-paced, dynamic environment with strict adherence to protocols.

  • Strong teamwork, adaptability, and communication skills.

  • Proficiency with electronic data capture systems and technology-driven workflows.

Physical & Work Environment Requirements

  • Ability to stand or remain stationary for 6–8 hours per day.

  • Repetitive hand movements for lab equipment operation.

  • Occasional crouching, stooping, bending, and twisting.

  • Ability to lift or move objects up to 15–20 lbs.

  • Flexible schedule and consistent attendance required.

Benefits

  • Comprehensive medical, dental, vision, life, STD/LTD insurance for full-time employees.

  • 401(k) retirement plan.

  • Paid time off (PTO) and employee recognition programs.

  • Employee Resource Groups (ERG) fostering professional growth and community engagement.

Why Join Us
This position provides the opportunity to engage directly with participants, develop clinical expertise, and contribute to innovative medical research. Your work will have a tangible impact on patients globally as investigational drugs progress from trials to approval.

EEO Statement
We are an equal opportunity employer and provide accommodations upon request.

How to Apply
Interested candidates can apply through our global portal at thepharmadaily.com to join a leading team advancing clinical research worldwide.