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Clinical Research Nurse

ICON PLC
2+ years
Not Disclosed
Statesville, North Carolina
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Clinical Research Nurse (Clinical Research Coordinator Nurse)

Location: Statesville, North Carolina, USA (Onsite)
Organization: ICON plc – Accellacare Clinical Research Network
Employment Type: Full-Time
Work Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Work Model: 100% Onsite


Job Summary

The Clinical Research Nurse (CRC Nurse) is responsible for coordinating and conducting clinical trial activities in accordance with study protocols, Good Clinical Practice (GCP), regulatory requirements, and site procedures.

The role combines direct patient care with clinical research coordination responsibilities, ensuring high-quality data collection, participant safety, protocol compliance, and successful execution of clinical studies. The Clinical Research Nurse serves as a key liaison between study participants, investigators, sponsors, and multidisciplinary research teams.


Key Responsibilities

Clinical Trial Coordination

  • Coordinate and manage clinical trial activities according to approved study protocols.

  • Schedule participant visits and study-related procedures.

  • Ensure protocol compliance throughout all study phases.

  • Maintain accurate study documentation and research records.

  • Assist investigators with study conduct and participant management.


Clinical Procedures & Patient Care

Perform protocol-specific clinical and nursing procedures, including:

  • Venipuncture and blood collection

  • Specimen processing and handling

  • Vital signs assessment

  • Electrocardiograms (ECGs/EKGs)

  • Holter monitoring

  • Pulmonary function testing

  • Allergy testing

  • Urine and serum pregnancy testing

  • Strep throat screening

  • Intramuscular (IM) injections

  • Subcutaneous (SQ) injections

  • Other study-related clinical procedures as required by protocol

  • Monitor participant safety and wellbeing throughout study participation.

  • Provide nursing care and medical support to study participants.

  • Identify and report adverse events and safety concerns appropriately.


Participant Recruitment & Enrollment

  • Assist with participant recruitment initiatives.

  • Screen potential participants against inclusion and exclusion criteria.

  • Conduct informed consent processes according to GCP requirements.

  • Facilitate participant enrollment and retention activities.

  • Maintain positive participant relationships throughout study participation.


Data Collection & Documentation

  • Collect, review, and document study-related data accurately and completely.

  • Ensure source documentation is maintained according to regulatory standards.

  • Enter study data into electronic data capture systems.

  • Resolve data discrepancies and support monitoring activities.

  • Maintain confidentiality of participant information.


Regulatory & Quality Compliance

  • Ensure compliance with:

    • Good Clinical Practice (GCP)

    • Institutional Review Board (IRB) requirements

    • FDA regulations

    • Study protocols

    • Sponsor requirements

    • Site Standard Operating Procedures (SOPs)

  • Support monitoring visits, audits, and inspections.

  • Maintain study regulatory binders and essential documents.

  • Assist with protocol deviation management and corrective actions.


Cross-Functional Collaboration

Collaborate effectively with:

  • Principal Investigators

  • Sub-Investigators

  • Clinical Research Coordinators

  • Sponsors

  • Clinical Research Associates (CRAs)

  • Laboratory Personnel

  • Regulatory Teams

  • Site Operations Staff

  • Participate in study meetings and research team discussions.

  • Ensure efficient communication across all stakeholders.


Educational Qualifications

Required

  • Bachelor's Degree in Nursing (BSN) or equivalent nursing qualification.

Licensure

  • Licensed Practical Nurse (LPN) – Required

  • Registered Nurse (RN) – Preferred