Overnight Clinical Research Nurse (PRN)

ICON plc•Lenexa, KS
•Onsite

About The Position

As a Clinical Research Nurse at ICON, you will support clinical trials by providing direct patient care and helping ensure the safety and well-being of research participants. This onsite overnight role supports studies involving investigational products and intensive participant monitoring. You will deliver high-quality research nursing care while following study protocols and maintaining participant safety during overnight operations.

Requirements

  • Associate's or Bachelor's degree in Nursing or a healthcare-related field.
  • Active Registered Nurse (RN) license in good standing.
  • Knowledge of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP).
  • Experience administering medications and assessing patient responses.
  • Strong attention to detail and ability to recognize and respond to adverse events.
  • Excellent communication and documentation skills.
  • Ability to work independently and collaboratively in a fast-paced clinical research setting.
  • Ability and willingness to work overnight shifts.

Nice To Haves

  • Clinical research experience or experience working in a regulated healthcare environment is preferred.

Responsibilities

  • Administer investigational products according to study protocols and physician orders.
  • Monitor research participants during dosing procedures and throughout study participation.
  • Identify, assess, document, and report adverse events and other safety findings in accordance with study protocols and regulatory requirements.
  • Perform clinical assessments, collect vital signs and samples, and complete other protocol-required procedures.
  • Collaborate with physicians, research staff, and multidisciplinary teams to ensure protocol compliance and participant safety.
  • Document study activities accurately and maintain research records in accordance with Good Clinical Practice (GCP) guidelines.
  • Educate and support study participants throughout their clinical trial experience.
  • Support overnight clinical operations while maintaining high standards of patient care and data quality.

Benefits

  • Competitive base salary and performance-related incentives.
  • Medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development opportunities through structured training and career pathways.
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