Clinical Research Coordinator Nurse
- Location
- Salisbury, NC · On-site
- Job type
- Full-time
- Level
- Mid-level
- Education
- Bachelor's degree
- Listed
- 30 days ago
Skills & highlights for this role
- LPN license
- GCP guidelines
- venipuncture
- clinical trial protocol procedures
- specimen processing
Also useful
- ECG
- pulmonary function testing
Stated benefits & perks
- Health
- Dental
- Vision
- Retirement
About the role
Clinical Research Coordinator Nurse - Salisbury, NC (Onsite) 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.
We have an incredible opportunity for a Clinical Research Coordinator Nurse (CRC Nurse) to join ICON's Accellacare team. The CRC Nurse is responsible for completing trial assignments in an autonomous, accurate, and timely manner. The CRC Nurse is performing technical and clinical requirements of study protocols as ordered by the investigator.
This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Location: 100% Onsite at Accellacare (410 Mocksville Avenue, Salisbury, NC, 28144) Hours: Monday - Friday; 8:00am - 5:00pm (no weekends or holidays) What you will be doing: Coordinating and conducting clinical trial procedures according to protocol requirements Performing technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator Collecting and documenting patient data accurately and efficiently Assisting in patient recruitment, screening, and enrollment processes Providing nursing care and support to trial participants Collaborating with interdisciplinary teams to ensure trial compliance and quality data collection Your profile: Bachelor's degree in Nursing or equivalent qualification LPN required, RN preferred Prior experience in clinical research coordination (preferred) Strong understanding of GCP guidelines and regulatory requirements Excellent communication skills Organizational skills with attention to detail Problem-solving skills #LI-Onsite #LI-TP1 #LI-Accellacare Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include: 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 Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. Are you a current ICON Employee? Please click here to apply
Equal opportunity and legal notices
Inclusion and Accessibility ICON is an equal opportunity employer. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
From ICON's careers page, first listed on Rolev.ai on October 10, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Clinical Research Coordinator Nurse job at ICON located?
This Clinical Research Coordinator Nurse position at ICON is located in Salisbury, NC (On-site). Always check ICON's application page for specific state eligibility or relocation policies.
What qualifications are required for Clinical Research Coordinator Nurse at ICON?
For the Clinical Research Coordinator Nurse role, ICON highlights a bachelor's degree; experience with GCP guidelines, venipuncture, clinical trial protocol procedures, specimen processing. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Clinical Research Coordinator Nurse position at ICON?
This listing links directly to ICON's Workday application page. You can apply directly on ICON's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.