Clinical Research Coordinator - Raleigh, NC
IQVIA•Parsippany, NJ
•Onsite
About The Position
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.
Requirements
- 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
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
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
