Clinical Research Coordinator I — On-Site, Multi-Trial Exposure

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

Job summary

IQVIA is partnering with Avacare to recruit a Clinical Research Coordinator for a fully on-site role in Elkhorn, Nebraska. You will manage patient recruitment, informed consent, and regulatory documentation while coordinating multiple trials under supervision.

As a CRC I/II, you will gain exposure to various therapeutic areas, work with investigators and sponsors, and contribute to site audits and data quality using CTMS and eCRFs.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and lab specimen processing.
• Solid understanding of site operations and drug development process.
• CRC I: 1–3 years in clinical research; CRC II: 3+ years as CRC at a clinical site.
• Strong written and verbal communication with attention to detail.
• Proficient with CTMS, eCRFs, and MS Office tools.

Responsibilities

• Manage 2–6 trials of varying complexity and lead study coordination.
• Coordinate patient recruitment and informed consent processes.
• Ensure regulatory documentation and site audits are completed accurately.
• Collaborate with investigators, sponsors, and monitors to advance trials.

Skills

Clinical Skills

Site Operations

CRC experience

Communication

CTMS/eCRFs

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is partnering with Avacare to recruit a Clinical Research Coordinator for a fully on-site role in Elkhorn, Nebraska. You will manage patient recruitment, informed consent, and regulatory documentation while coordinating multiple trials under supervision.

As a CRC I/II, you will gain exposure to various therapeutic areas, work with investigators and sponsors, and contribute to site audits and data quality using CTMS and eCRFs.