Clinical Research Coordinator

Responsibilities

• Coordinate and conduct clinical research activities in accordance with study protocols, GCP, and regulatory requirements
• Perform study-related clinical procedures including ECGs, vital signs, and biological sample collection
• Conduct patient visits including screening, enrollment, education, orientation, and follow-up
• Support patient recruitment efforts and community outreach
• Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs)
• Request, review, and manage medical records to support study eligibility
• Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality
• Maintain a safe clinical environment and serve as a patient advocate

Requirements

• Minimum of 1+ year of clinical research coordination experience
• Hands-on experience with EDC data entry and query resolution
• Experience with collection, processing, and shipping of laboratory samples
• Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
• Experience with chart pre-screening and patient pre-screening activities
• Strong organizational skills and attention to detail

Preferred Qualifications

• Bachelor's degree
• Bilingual in English and Spanish (written and verbal)

About the Company

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide.