Clinical Research Coordinator Nurse

ICON; Knoxville (TN); On-site; USD 60,000 - 80,000; Full time

Job summary

ICON is seeking a Clinical Research Coordinator Nurse in Knoxville, TN. In this role, you will coordinate clinical trials, collect patient data, and provide nursing care, ensuring compliance and quality data collection. Ideal candidates will have a Bachelor's in Nursing and RN or LPN licensure, with prior clinical research experience preferred.

Benefits

Various annual leave entitlements

Health insurance options for you and your family

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• RN or LPN licensure required.
• Prior experience in clinical research coordination preferred.
• Strong understanding of GCP guidelines and regulatory requirements.

Responsibilities

• Coordinating and conducting clinical trial procedures according to protocol requirements.
• Collecting and documenting patient data accurately and efficiently.
• Assisting in patient recruitment, screening, and enrollment processes.

Skills

Communication

Organizational skills

Problem-solving

Education

Bachelor's degree in Nursing

Job description

Clinical Research Coordinator Nurse

ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence, and we welcome you to join us in shaping the future of clinical development.

We are seeking a Clinical Research Coordinator Nurse to join our diverse and dynamic team in Knoxville, TN. As a CRC Nurse, you will play a key role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments and therapies.

Title: Clinical Research Coordinator Nurse (CRC Nurse)

Location: 100% on-site in Knoxville, TN

Responsibilities include:

1. Coordinating and conducting clinical trial procedures according to protocol requirements
2. Collecting and documenting patient data accurately and efficiently
3. Assisting in patient recruitment, screening, and enrollment processes
4. Providing nursing care and support to trial participants
5. Collaborating with interdisciplinary teams to ensure trial compliance and quality data collection

Your profile:

• Bachelor's degree in Nursing or an equivalent qualification
• RN or LPN licensure
• Prior experience in clinical research coordination preferred
• Strong understanding of GCP guidelines and regulatory requirements
• Excellent communication, organizational, and problem-solving skills

#LI-SB4

#LI-onsite

What ICON can offer you:

Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options for you and your family
• Retirement planning options to maximize savings
• Global Employee Assistance Programme, LifeWorks, providing 24-hour support from over 80,000 professionals
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, and more

Visit our careers site to learn more about ICON's benefits.

At ICON, inclusion and belonging are core to our culture. We are committed to providing an accessible, discrimination-free workplace. Qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know or submit a request here.

Interested but unsure if you meet all requirements? We encourage you to apply—your skills may be exactly what we’re looking for.

If you are a current ICON employee, please apply here.