On-Site CRC I: Multi-Trial Clinical Research

IQVIA; Omaha (NE); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA is seeking a hands-on Clinical Research Coordinator for an on-site role in the Omaha, NE area. You will support site activities across multiple trials, manage patient coordination, and ensure regulatory documentation compliance in a fast-paced SMO environment.

The role emphasizes direct patient interaction, data entry via CTMS/eCRFs, and collaboration with investigators and monitors to maintain study timelines and quality.

Qualifications

• CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
• CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
• Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management.
• Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Skills

Vital signs

Phlebotomy

ECGs

Lab processing

Tools

CTMS

eCRFs

MS Office

Job description

IQVIA is seeking a hands-on Clinical Research Coordinator for an on-site role in the Omaha, NE area. You will support site activities across multiple trials, manage patient coordination, and ensure regulatory documentation compliance in a fast-paced SMO environment.

The role emphasizes direct patient interaction, data entry via CTMS/eCRFs, and collaboration with investigators and monitors to maintain study timelines and quality.