On-Site CRC I: Grow with Diverse Trials

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

Job summary

IQVIA is seeking a Clinical Research Coordinator for a fully on-site role in Elkhorn, Nebraska. The CRC will manage multiple trials, perform vital clinical procedures, and coordinate study activities from recruitment to regulatory documentation.

The position emphasizes collaboration with investigators, sponsors, and monitors, with opportunities to mentor junior staff and grow within clinical operations. Experience with CTMS/eCRFs and MS Office is required.

Qualifications

• Hands-on experience obtaining vital signs, phlebotomy, ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC I: 1–3 years at a clinical investigative site; CRC II: 3+ years as a CCR at a clinical investigative site.
• Excellent written and verbal communication with strong time-management skills.
• Proficient using CTMS, eCRFs, and MS Office tools.

Responsibilities

• Manage multiple trials (2–6) across varying complexity from start to finish.
• Coordinate study activities, ensure regulatory documentation and patient recruitment.
• Collaborate with investigators, sponsors, and monitors and mentor junior staff.
• Ensure data quality and compliance with trial protocols and regulations.

Skills

Clinical Skills

Site Operations Knowledge

Communication & Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking a Clinical Research Coordinator for a fully on-site role in Elkhorn, Nebraska. The CRC will manage multiple trials, perform vital clinical procedures, and coordinate study activities from recruitment to regulatory documentation.

The position emphasizes collaboration with investigators, sponsors, and monitors, with opportunities to mentor junior staff and grow within clinical operations. Experience with CTMS/eCRFs and MS Office is required.