Clinical Research Nurse (Part-Time Day Shift), Onsite, Salt Lake City, UT

ICON plc • Salt Lake City, UT

6d • Onsite

About The Position

As a Clinical Research Nurse I at ICON, you will support the execution of clinical trials, ensuring adherence to protocol requirements and providing compassionate patient care throughout the research process. The role involves delivering clinical research operations work to a high standard and working closely with the team and stakeholders.

You will assist with planning, implementing, and coordinating clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures. You will conduct patient assessments, administer study treatments, perform protocol-required clinical procedures, and support patient safety and ethical standards. The role also involves collecting and maintaining accurate study documentation and data, collaborating with multidisciplinary teams to support study conduct and participant recruitment and retention, and educating and counseling participants and families about study procedures, treatment regimens, and informed consent.

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.
• 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 regulatory requirements, including International Council for Harmonisation (ICH) guidelines and local regulatory requirements, and commitment to ethical standards and patient confidentiality.
• Proficiency in electronic medical record systems, clinical documentation, and data entry, with strong attention to detail and accuracy.
• Excellent interpersonal and organizational skills, including the ability to work independently and collaboratively in a fast-paced, multidisciplinary environment, prioritize competing demands, and meet project deadlines.

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.
• Conduct patient assessments, administer study treatments, and perform clinical procedures required by the research protocol 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 and study databases.
• Collaborate with investigators, study coordinators, regulatory staff, and other multidisciplinary team members to support efficient study conduct, participant recruitment, and retention.
• Educate and counsel study participants and their families about study procedures, treatment regimens, and informed consent, and address questions or concerns.

Benefits

• 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.

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level