Overnight Clinical Research Nurse (PRN)

IRE • Lawrence, KS

1d • Onsite

About The Position

ICON is seeking an onsite Clinical Research Nurse I in Lenexa, Kansas, to support overnight clinical research studies involving investigational products and intensive participant monitoring. The nurse provides direct patient care while supporting study protocols and protecting research participants’ safety and well-being.

The role delivers clinical research nursing care during overnight operations, supports protocol compliance and data quality, and educates and supports participants throughout their clinical trial experience.

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.

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.
• 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 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.

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level
• Education Level: Associate degree