Clinical Research Coordinator Nurse

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 requirementsPerforming 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 investigatorCollecting and documenting patient data accurately and efficientlyAssisting in patient recruitment, screening, and enrollment processesProviding nursing care and support to trial participantsCollaborating with interdisciplinary teams to ensure trial compliance and quality data collectionYour profile:Bachelor's degree in Nursing or equivalent qualificationLPN required, RN preferredPrior experience in clinical research coordination (preferred)Strong understanding of GCP guidelines and regulatory requirementsExcellent communication skillsOrganizational skills with attention to detailProblem-solving skillsEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.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 incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Visit our careers site to read more about the benefits ICON offers.ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.