Clinical Research Coordinator – Raleigh, NC

Work Setup: On-site
Employment Type: Full-time

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