On-Site CRC I: Lead & Coordinate Diverse Trials

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

Job summary

Avacare, an SMO, seeks a Clinical Research Coordinator for an entirely on-site role in Elkhorn, Nebraska. You will gain exposure to multiple trials, perform core clinical procedures, and collaborate with investigators and sponsors to advance patient care.

You will manage study coordination, regulatory tasks, and data entry across CTMS and eCRFs while mentoring junior staff and contributing to team training. This position offers hands-on growth in a dynamic clinical research environment.

Qualifications

• Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC I: 1–3 years in a clinical research site; CRC II: 3 years as a CRC in a clinical investigative site.

Responsibilities

• Manage 2–6 trials of varying complexity and lead study coordination from start to finish.
• Recruit patients and obtain informed consent.
• Maintain regulatory documentation and assist with site audits.

Skills

Vital signs

Phlebotomy

ECGs

Lab processing

CTMS

eCRFs

Microsoft Office

Tools

CTMS

eCRFs

Microsoft Office

Job description

Avacare, an SMO, seeks a Clinical Research Coordinator for an entirely on-site role in Elkhorn, Nebraska. You will gain exposure to multiple trials, perform core clinical procedures, and collaborate with investigators and sponsors to advance patient care.

You will manage study coordination, regulatory tasks, and data entry across CTMS and eCRFs while mentoring junior staff and contributing to team training. This position offers hands-on growth in a dynamic clinical research environment.