Clinical Trial Nurse – Augusta, GA

Work Setup: On-site
Schedule: Part-time, 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to advancing healthcare. 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, we generate high-quality insights that drive the future of clinical development.

About the Role

IQVIA is seeking a Clinical Trial Nurse to support the successful execution of clinical trials under the direction of a Principal Investigator. This is a hands-on role that blends patient-facing care, clinical procedures, and study coordination responsibilities while ensuring strict adherence to regulatory and quality standards.

Key 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

• Prepare study materials, maintain study documentation, and manage study logistics

• 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

• Support monitoring visits, audits, and regulatory inspections

• Act as a patient advocate, maintaining a safe and compliant research environment

• Engage in community outreach efforts to support patient recruitment

Qualifications

• Bachelor’s degree preferred or an equivalent combination of education and relevant experience

• At least 1+ year of hands-on clinical research experience in a clinical or site setting

• Demonstrated experience coordinating clinical trials, including data entry and query resolution

• Strong understanding of Good Clinical Practice (GCP), clinical trial processes, and medical terminology

• Experience performing clinical procedures such as phlebotomy and medication/drug administration

• Proficiency with EDC systems and a high level of accuracy in data management

• Strong organizational skills, attention to detail, and ability to build effective working relationships

Additional Information

• This is an on-site position based in Augusta, GA

• Sponsorship is not available for this role