Overnight Clinical Research Nurse (PRN)

ICON Clinical Research; Lenexa (KS); Vor Ort; USD 55.000 - 90.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme

Zusammenfassung

ICON Clinical Research in Lenexa, KS is seeking an Overnight Clinical Research Nurse I (Onsite) to provide direct patient care during overnight trials. You will administer investigational products, monitor dosing, assess and report adverse events, and ensure participant safety while maintaining high data quality.

The role requires an Associate’s or Bachelor’s degree in Nursing, an active RN license, and knowledge of GCP and clinical trial processes.

Qualifikationen

• Bachelor’s or Associate’s degree in Nursing.
• Active RN license in good standing.
• Clinical research experience or regulated healthcare environment preferred.
• Knowledge of clinical trial processes and GCP.

Aufgaben

• Deliver nursing care in alignment with study protocols.
• Monitor participants during overnight dosing and study participation.
• Identify, assess, and report adverse events per protocol and regulatory requirements.
• Perform clinical assessments, vital signs collection and specimen collection.
• Collaborate with physicians and research staff to ensure protocol compliance.
• Accurately document study activities and maintain records per GCP.
• Educate and support participants throughout the trial experience.
• Support overnight operations while maintaining high patient care and data quality.

Kenntnisse

Attention to detail

Documentation

Communication

Independence

Team collaboration

Overnight shift

Ausbildung

Associate's or Bachelor's degree in Nursing

Active RN license

Jobbeschreibung

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

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 values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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. This is an overnight position supporting clinical research studies involving investigational products and intensive patient monitoring.

What You Will Do:

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.

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What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply