IQVIA
life sciences
ClinicalResearchCoordinator
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“Clinical Research Coordinator at IQVIA. Skills: Clinical Research Coordinator, clinical trial execution, patient recruitment, data collection, regulatory compliance. 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”
What You'll Achieve.
successful execution of clinical trials; high-quality, audit-ready datasets
Industry & Context.
not eligible for visa sponsorship
What They're Looking For.
Must Have
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, 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
What You'll Do.
Perform clinical procedures including ECGs
and biological sample collection in accordance with study protocols
Coordinate daily clinical trial activities while ensuring compliance with GCP
and regulatory guidelines
Prepare study materials
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
and orient study participants throughout the clinical trial process
and enter clinical data into EDC systems and case report forms (CRFs)
Perform data review and resolve queries to maintain high-quality
Collaborate with investigators
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
How You'll Work.
Team & Collaboration
Collaborate with investigators, sponsors, and monitors; ability to collaborate cross-functionally
Communication Scope
Effective communication and interpersonal skills
Full Job Description
# **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 hea
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