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Clinical Research Nurse /Madison, Wi (On-Site)

Fortrea
Fortrea
0-1 years
preferred by company
10 Jan. 6, 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

Clinical Research Nurse – Onsite – Madison, WI

Location: Madison, Wisconsin
Job Type: Full-Time, Onsite
Experience Required: 0–1 year (entry-level)
Category: Patient Services / Clinical Research
Job ID: 253969


About Fortrea

Fortrea is a global leader in early-phase clinical research, operating four Phase I Clinical Research Units across the US and UK. We partner with top pharmaceutical, biotechnology, and medical device companies to conduct innovative clinical trials that advance drug development and patient care.

We are seeking a Clinical Research Nurse to join our Madison, WI Phase I site. This onsite role offers hands-on experience with healthy volunteer participants, exposure to diverse therapeutic areas, and training in clinical research protocols.


Role Overview

As a Clinical Research Nurse, you will provide high-quality care to participants, support the execution of clinical trials, and contribute to accurate and compliant study documentation. This role is ideal for early-career nurses looking to specialize in clinical research while gaining exposure to Phase I studies, including first-in-human, ascending dose, food effect, and drug-drug interaction trials.


Key Responsibilities

  • Deliver safe, compassionate, and protocol-compliant nursing care to clinical trial participants.

  • Monitor participants’ health, document observations, and identify adverse events; take appropriate clinical actions as required.

  • Obtain informed consent and educate participants about study procedures, risks, and benefits.

  • Administer investigational products, including parenteral compounds, according to protocol and regulatory standards.

  • Perform clinical procedures including cannulation, telemetry, ECGs, holter monitoring, vital signs, and venipuncture.

  • Respond promptly to emergency situations in accordance with nursing standards and facility protocols.

  • Maintain accurate and complete clinical documentation for regulatory compliance.

  • Participate in study-related meetings, training, and continuous professional development.

  • Undertake additional responsibilities as required to support the clinical team and study objectives.


Required Qualifications

  • Associate’s or Bachelor’s Degree in Nursing with active licensure in the applicable state.

  • CPR/AED certification; ACLS certification preferred (may be obtained during role if not yet certified).

  • 0–1 year of clinical nursing experience; prior clinical research experience is a plus.

  • Strong communication and interpersonal skills.

  • Commitment to patient safety, regulatory compliance, and professional development.


Work Environment & Physical Requirements

  • Work is performed onsite in a clinical and laboratory environment with standard office and lab equipment.

  • Exposure to biological fluids; personal protective equipment (PPE) required.

  • Ability to work upright or stationary for 6–8 hours per day.

  • Repetitive hand movements required for clinical procedures and equipment operation.

  • Occasional bending, stooping, crouching, and lifting up to 15–20 lbs.

  • Flexible hours and attendance required, based on study needs and participant schedules.


Key Attributes

  • Comfortable in a fast-paced, protocol-driven environment where timelines and accuracy are critical.

  • Able to prioritize and adapt to changing study requirements.

  • Strong teamwork and collaboration skills to support clinical operations.

  • Comfortable using technology to record study data and follow electronic protocols.


Benefits

  • Competitive salary based on experience.

  • Comprehensive benefits for full-time or part-time employees (20+ hours/week), including:

    • Medical, Dental, Vision, Life, STD/LTD insurance

    • 401(K) retirement plan

    • Paid Time Off (PTO)

    • Employee recognition programs

    • Participation in employee resource groups (ERGs)


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