Clinical Research Coordinator - Raleigh, NC

Clinical Research Coordinator - Raleigh, NCRaleigh, United States of America | Part time | Office-basedIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we deliver high-quality data and insights that shape the future of clinical trials.Position OverviewWe are seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical trials under the supervision of a Principal Investigator. This role requires a detail-oriented, patient-focused professional who can manage clinical, operational, and data-related responsibilities while ensuring compliance with regulatory and protocol requirements.Key ResponsibilitiesPerform clinical procedures including ECGs, vital signs, and biological sample collection in accordance with study protocolsCoordinate daily clinical trial activities while ensuring compliance with GCP, study protocols, and regulatory guidelinesPrepare study materials, maintain equipment, and support site readiness for study visitsConduct patient recruitment and pre-screening activities, including chart review and phone screeningsSchedule and conduct patient study visits, ensuring protocol adherence and participant safetyEducate, consent, and orient study participants throughout the clinical trial processAccurately collect, document, and enter clinical data into EDC systems and case report forms (CRFs)Perform data review and resolve queries to maintain high-quality, audit-ready datasetsCollaborate with investigators, sponsors, and monitors, including support during monitoring visits and auditsMaintain a safe clinical environment and serve as a patient advocate in accordance with health and safety standardsQualificationsBachelor's degree preferred or equivalent combination of education and relevant experienceMinimum of 1+ year of clinical research experience, including hands-on coordinating responsibilitiesDemonstrated experience conducting study visits, patient recruitment, and pre-screening activitiesProficiency in clinical data entry, including use of EDC systems and query resolutionWorking knowledge of clinical trial processes, GCP guidelines, and medical terminologyStrong attention to detail with the ability to manage multiple priorities in a fast-paced environmentEffective communication and interpersonal skills with the ability to collaborate cross-functionallyAdditional InformationThis position is not eligible for visa sponsorshipIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.