Clinical Research Coordinator - Somerset, NJ

divh2Clinical Research Coordinator - Somerset, NJ/h2pLinden, United States of America | Part time | Office-based/ppClinical Research Coordinator - Somerset, NJ Work Set-Up: On-site Scheduled Weekly Hours: 40 Hours per week/ppIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the worlds leading pharmaceutical, biotechnology, and medical device companies to drive healthcare forward. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that accelerate innovation and improve patient outcomes worldwide./ppAbout the Role/ppWe are seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator. This role plays a critical part in the successful execution of clinical trials, combining hands-on clinical procedures, patient interaction, and study coordination to ensure compliance, data integrity, and participant safety./ppKey Responsibilities/pulliPerform clinical procedures including ECGs, vital signs, and biological sample collection./liliCoordinate daily clinical research activities in compliance with study protocols and Good Clinical Practice (GCP) guidelines./liliPrepare and maintain study materials, equipment, and documentation to support study conduct./liliRecruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial./liliAccurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems./liliCollaborate closely with investigators, monitors, and study team members to resolve queries and maintain data quality./liliServe as a patient advocate while maintaining a safe clinical environment in accordance with Health and Safety policies./li/ulpQualifications/pulliBachelors degree preferred, or an equivalent combination of education and relevant experience./liliMinimum of 1+ year of experience in clinical research or a related healthcare setting./liliWorking knowledge of clinical trials, GCP principles, and medical terminology./liliExperience conducting study visits, including patient education and chart review./liliExposure to cardiovascular studies and related clinical procedures is preferred./liliFamiliarity with maintaining regulatory binders, managing study supplies, and updating study portals./liliStrong attention to detail with the ability to build effective working relationships./liliProficiency in EDC systems, accurate data entry, and query resolution./li/ulpIQVIA 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./ppIQVIA 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./p/div