Clinical Research Coordinator Nurse

About the role

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)

Responsibilities

• 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

Qualifications

• Bachelor's degree in Nursing or equivalent qualification
• LPN required
• RN preferred
• Prior experience in clinical research coordination (preferred)

Skills

• Strong understanding of GCP guidelines and regulatory requirements
• Excellent communication skills
• Organizational skills with attention to detail
• Problem-solving skills

Benefits

• 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