On-Site Clinical Research Coordinator: Diverse Trials

IQVIA; Las Vegas (NV); Hybrid; USD 41,000 - 102,000; Full time

Job summary

IQVIA in Las Vegas, NV is seeking a Clinical Research Coordinator for on-site support of multiple trials. The role involves hands-on clinical procedures, patient recruitment, informed consent, and regulatory documentation across diverse studies.

The candidate will work with a collaborative team, leveraging CTMS, eCRFs, and MS Office tools to maintain study integrity and ensure timely data capture and compliance.

Qualifications

• Hands-on clinical skills including vital signs, phlebotomy, ECGs, and specimen handling.
• Experience coordinating clinical trials and site activities.
• Strong documentation and communication skills for regulatory compliance.

Responsibilities

• Coordinate 2–6 trials across multiple therapeutic areas.
• Manage patient recruitment, informed consent, and site regulatory documentation.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimens

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA in Las Vegas, NV is seeking a Clinical Research Coordinator for on-site support of multiple trials. The role involves hands-on clinical procedures, patient recruitment, informed consent, and regulatory documentation across diverse studies.

The candidate will work with a collaborative team, leveraging CTMS, eCRFs, and MS Office tools to maintain study integrity and ensure timely data capture and compliance.