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Clinical Research Coordinator Nurse (Crc Nurse) – Accellacare | Icon Plc

Icon Plc
ICON PLC
0-2 years
$56,704 – $70,880 per yea
Illinois, USA, Lombard, United States
1 May 7, 2026
Job Description
Job Type: Full Time Education: Bachelor’s degree in Nursing or equivalent qualification Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Clinical Research Coordinator Nurse (CRC Nurse) – Accellacare | ICON plc

Company: ICON plc
Division: Accellacare – ICON Clinical Research Network
Job Title: Clinical Research Coordinator Nurse (CRC Nurse)
Location: Winfield, Illinois & Lombard, Illinois, USA
Job Type: Full-Time
Work Mode: On-Site
Work Schedule: Monday – Friday | 8:00 AM – 5:00 PM ET
Salary Range: $56,704 – $70,880 per year
Job Requisition ID: JR147845


About ICON plc & Accellacare

ICON plc is a globally recognized Clinical Research Organization (CRO) specializing in healthcare intelligence, clinical development, and innovative clinical trial solutions. Through its Accellacare clinical site network, ICON delivers patient-focused clinical research services designed to improve trial efficiency, patient access, and study outcomes.

Accellacare combines advanced clinical operations with high-quality patient care to support pharmaceutical, biotechnology, and healthcare companies worldwide.


Job Overview

ICON plc is hiring a Clinical Research Coordinator Nurse (CRC Nurse) to support clinical trial operations at Accellacare research sites in Illinois.

The Clinical Research Coordinator Nurse will be responsible for:

  • Conducting clinical trial procedures
  • Supporting patient recruitment and enrollment
  • Performing protocol-specific nursing procedures
  • Ensuring clinical trial compliance
  • Maintaining accurate patient documentation
  • Delivering high-quality patient care during clinical studies

This role is ideal for nurses interested in clinical research, patient care, and clinical trial coordination within a fast-growing CRO environment.


Experience Required

Preferred Experience

  • Prior experience in:
    • Clinical Research Coordination
    • Clinical Trials
    • Research Nursing
    • Patient Care Operations

Freshers Eligibility

  • Freshers with nursing qualifications may apply
  • Candidates with prior clinical research experience will have an advantage

Educational Qualification

Required Qualification

  • Bachelor’s degree in Nursing or equivalent qualification

Licensure Requirements

  • LPN (Licensed Practical Nurse) – Required
  • RN (Registered Nurse) – Preferred

Key Responsibilities

Clinical Trial Coordination

  • Coordinate and conduct study-related clinical procedures
  • Ensure protocol compliance during all research activities
  • Support investigators and research teams throughout clinical trial execution

Patient Care & Nursing Procedures

Perform protocol-specific procedures including:

  • Venipuncture
  • Specimen collection and processing
  • Vital signs monitoring
  • Electrocardiograms (ECG/EKG)
  • Holter monitoring
  • Pulmonary function testing
  • Allergy testing
  • Pregnancy testing
  • Strep throat screening
  • Injections (IM/SQ)

Patient Recruitment & Enrollment

  • Assist with:
    • Patient screening
    • Recruitment
    • Enrollment processes
  • Educate participants regarding study procedures and protocols

Clinical Documentation

  • Accurately collect and document patient data
  • Maintain study records according to:
    • GCP guidelines
    • Regulatory requirements
    • Study protocols

Cross-Functional Collaboration

  • Work closely with:
    • Investigators
    • Research coordinators
    • Clinical staff
    • Sponsors
    • Site management teams