Clinical Research Coordinator - Raleigh, NC

Clinical Research Coordinator - Raleigh, NC Raleigh, United States of America | Part time | Office-based | R1544819 About IQVIA IQVIA 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 Overview We 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 Responsibilities Perform clinical procedures including ECGs, vital signs, and biological sample collection in accordance with study protocols Coordinate daily clinical trial activities while ensuring compliance with GCP, study protocols, and regulatory guidelines Prepare study materials, maintain equipment, and support site readiness for study visits Conduct patient recruitment and pre-screening activities, including chart review and phone screenings Schedule and conduct patient study visits, ensuring protocol adherence and participant safety Educate, consent, and orient study participants throughout the clinical trial process Accurately 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 datasets Collaborate with investigators, sponsors, and monitors, including support during monitoring visits and audits Maintain a safe clinical environment and serve as a patient advocate in accordance with health and safety standards Qualifications Bachelor’s degree preferred or equivalent combination of education and relevant experience Minimum of 1+ year of clinical research experience, including hands‑on coordinating responsibilities Demonstrated experience conducting study visits, patient recruitment, and pre‑screening activities Proficiency in clinical data entry, including use of EDC systems and query resolution Working knowledge of clinical trial processes, GCP guidelines, and medical terminology Strong attention to detail with the ability to manage multiple priorities in a fast-paced environment Effective communication and interpersonal skills with the ability to collaborate cross‑functionally Additional Information This position is not eligible for visa sponsorship The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a proud 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. We appreciate your honesty and professionalism. #J-18808-Ljbffr IQVIA Argentina