Clinical Research Coordinator

Responsibilities

• Perform clinical procedures including ECGs, vital signs, and biological sample collection
• Coordinate daily clinical research activities in compliance with study protocols and Good Clinical Practice (GCP) guidelines
• Recruit, screen, consent, and orient study participants to ensure a safe patient experience
• Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems
• Prepare and maintain study materials, equipment, and regulatory documentation
• Collaborate with investigators and monitors to resolve data queries and maintain quality standards

Requirements

• Minimum of 1+ year of experience in clinical research or a related healthcare setting
• Working knowledge of clinical trials, GCP principles, and medical terminology
• Proficiency in EDC systems, accurate data entry, and query resolution
• Experience conducting study visits, including patient education and chart review
• Bachelor’s degree preferred, or an equivalent combination of education and experience

Preferred Qualifications

• Exposure to cardiovascular studies and related clinical procedures
• Experience maintaining regulatory binders and managing study supplies

About the Company

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to drive healthcare forward by combining deep scientific expertise with cutting-edge technology to improve patient outcomes worldwide.