Clinical Research Nurse

• Clinical Research Coordinator Nurse - Raleigh, 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 (3700
• Barrett
• Drive,
• Suite 310
• Raleigh,
• NC 27609)
• 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.