Clinical Research Nurse (Overnight, Part-Time) - Salt Lake City, UT

ICON plc • Salt Lake City, UT

6d

About The Position

As a Clinical Research Nurse I at ICON, you will support the execution of clinical trials, ensure adherence to study protocols, and provide compassionate patient care throughout the research process. You will deliver clinical research operations work to a high standard while working closely with your team and stakeholders. The role is overnight and part-time in Salt Lake City, Utah.

Requirements

• Bachelor's degree in Nursing (BSN) from an accredited institution.
• Current Registered Nurse (RN) licensure in the applicable jurisdiction.
• Minimum of 1–2 years of clinical nursing experience; research or academic healthcare experience is preferred, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.
• Strong clinical assessment and critical thinking skills, including the ability to recognize and respond to changes in patient status and communicate effectively with healthcare professionals and study investigators.
• Knowledge of clinical research regulations, including International Council for Harmonisation (ICH) guidelines and local requirements, and commitment to ethical standards and patient confidentiality.
• Proficiency in electronic medical record (EMR) systems, clinical documentation, and data entry, with strong attention to detail and accuracy.
• Excellent interpersonal and organizational skills, and ability to work independently and collaboratively in a fast-paced, multidisciplinary environment while prioritizing competing demands and meeting project deadlines.
• Legal right to work in the country where the role is based.

Nice To Haves

• Clinical nursing experience in a research or academic healthcare setting.
• Exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.

Responsibilities

• Assist in planning, implementing, and coordinating clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures (SOPs).
• Conduct patient assessments, administer study treatments, and perform clinical procedures required by research protocols while ensuring patient safety and compliance with ethical standards.
• Collect, record, and maintain accurate and complete documentation, including medical histories, vital signs, adverse events, and laboratory results, in electronic case report forms (eCRFs) and study databases.
• Collaborate with investigators, study coordinators, regulatory staff, and other multidisciplinary team members to support efficient study conduct, participant recruitment, and retention throughout the trial.
• Educate and counsel study participants and their families about study procedures, treatment regimens, and informed consent, and address questions or concerns during the study.

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