Clinical Research Coordinator

Responsibilities

• Perform clinical procedures including ECGs, vital signs, and biological sample collection
• Coordinate daily clinical trial activities ensuring compliance with GCP and study protocols
• Conduct patient recruitment, pre-screening, chart reviews, and phone screenings
• Schedule and conduct patient study visits while ensuring participant safety
• Educate, consent, and orient study participants throughout the trial process
• Collect, document, and enter clinical data into EDC systems and case report forms
• Perform data review and resolve queries to maintain audit-ready datasets
• Collaborate with investigators, sponsors, and monitors during site visits and audits

Requirements

• 1+ year of clinical research experience, including hands-on coordinating responsibilities
• Bachelor's degree preferred or equivalent combination of education and experience
• Demonstrated experience in patient recruitment and conducting study visits
• Proficiency in clinical data entry and the use of EDC systems
• Working knowledge of GCP guidelines and medical terminology
• Strong attention to detail and ability to manage multiple priorities

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 advanced technology.