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From the employer's careers site First seen 2 Nov 2026

Overnight Clinical Research Nurse I (Onsite) - Lenexa, KS

ICON Lenexa On-site part-time

The employer hasn't listed a salary.

Apply on ICON

Description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Clinical Research Nurse at ICON, you will play a critical role in the execution of clinical trials, providing direct patient care while ensuring the safety and well-being of research participants.

Responsibilities

You will be responsible for delivering high-quality clinical research nursing care while supporting study protocols and participant safety during overnight operations.

Key responsibilities include:

  • 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, vital signs collection, sample collection, and other protocol-required procedures.
  • Collaborate with physicians, research staff, and multidisciplinary teams to ensure protocol compliance and participant safety.
  • Accurately document study activities 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 a high standard of patient care and data quality.

Your Profile

You will bring relevant nursing and clinical research experience, along with the following qualifications and skills:

Required Qualifications and Experience:

  • Associate's or Bachelor's degree in Nursing or a healthcare-related field.
  • Active Registered Nurse (RN) license in good standing.
  • Clinical research experience or experience working in a regulated healthcare environment preferred.
  • 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.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including 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

Skills

Required

Nice to have

  • clinical research experience
  • regulated healthcare environment experience

Ready to apply?

You apply with the employer directly. Their original posting is here: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Lenexa-KCI-PRA/Overnight-Clinical-Research-Nurse--PRN-_JR162759-1

Apply on ICON