Clinical Research Coordinator

Responsibilities

• Perform clinical procedures including ECGs, vital signs, and biological sample collection
• Coordinate day-to-day clinical trial activities ensuring compliance with GCP and regulatory requirements
• Conduct patient recruitment activities such as chart reviews, phone screenings, and scheduling
• Manage patient study visits and educate participants to ensure safety and high standards of care
• Accurately collect, document, and enter data into EDC systems and case report forms
• Resolve data queries promptly and maintain high data quality standards
• Collaborate with investigators, sponsors, and monitors during site visits and audits

Requirements

• Minimum of 1+ years of clinical research experience in a coordinator or similar role
• Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
• Experience in patient recruitment, including chart review and phone screenings
• Proficiency with EDC systems, including accurate data entry and query resolution
• Bachelor's degree preferred, or an equivalent combination of education and experience
• Strong attention to detail and ability to manage multiple priorities

Preferred Qualifications

• Cardiovascular research experience

About the Company

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation by combining deep scientific expertise with cutting-edge technology.