Clinical Research Coordinator I - On-Site, Multitrial Exposure

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

Job summary

IQVIA seeks Clinical Research Coordinators for an on-site role in the Elkhorn/Omaha area. You will manage patient recruitment, informed consent, regulatory documentation, and site audits across multiple trials, collaborating with investigators and sponsors.

The position offers hands-on exposure to CTMS, eCRFs, and diverse therapeutic areas, with a strong emphasis on documentation, compliance, and team mentorship. On-site in Nebraska.

Qualifications

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

Responsibilities

• Coordinate 2–6 trials of varying complexity from start to finish.
• Recruit patients and obtain informed consent.
• Manage regulatory documentation and site audits.
• Collaborate with investigators, sponsors, and monitors.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimen handling

Communication

Documentation

CTMS

eCRFs

Microsoft Office

Education

CRC I: 1–3 years

CRC II: 3+ years

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA seeks Clinical Research Coordinators for an on-site role in the Elkhorn/Omaha area. You will manage patient recruitment, informed consent, regulatory documentation, and site audits across multiple trials, collaborating with investigators and sponsors.

The position offers hands-on exposure to CTMS, eCRFs, and diverse therapeutic areas, with a strong emphasis on documentation, compliance, and team mentorship. On-site in Nebraska.