Clinical Trial Nurse

Responsibilities

• Perform clinical procedures including phlebotomy, drug administration, ECGs, vital signs, and biological sample collection
• Coordinate day-to-day clinical trial activities in compliance with protocols, GCP, and site procedures
• Recruit, screen, consent, and educate study participants while ensuring safety and protocol adherence
• Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems
• Resolve data queries in collaboration with monitors and sponsors to ensure data integrity
• Prepare study materials, maintain documentation, and manage study logistics
• Support monitoring visits, audits, and regulatory inspections
• Act as a patient advocate to maintain a safe and compliant research environment

Requirements

• At least 1+ year of hands-on clinical research experience in a clinical or site setting
• Demonstrated experience with phlebotomy and medication/drug administration
• Strong understanding of Good Clinical Practice (GCP) and medical terminology
• Proficiency with EDC systems and high accuracy in data management
• Strong organizational skills and attention to detail

Preferred Qualifications

• Bachelor's degree in a related field

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 accelerate innovation and improve patient outcomes by combining deep scientific expertise with cutting-edge technology.