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

IQVIA; Papillion (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 Nebraska. You will gain exposure to multiple trials, manage site operations, and work closely with investigators and sponsors to ensure protocol adherence and patient safety.

The ideal candidate has hands-on clinical skills, experience with CTMS/eCRFs, and a track record of accurate regulatory documentation. This position offers a collaborative, fast-paced environment in a local SMO with global CRO backing.

Qualifications

• Hands-on experience in 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 site; CRC II: 3+ years as CRC with participants.
• Strong written and verbal communication with time management.
• Proficient with CTMS, eCRFs and MS Office tools.

Responsibilities

• Manage 2–6 trials of varying complexity and lead study coordination end-to-end.
• Coordinate patient recruitment, informed consent and study activities.
• Maintain regulatory documentation and support site audits.
• Collaborate with investigators, sponsors and monitors; mentor junior staff.

Skills

Clinical skills

Site operations

Communication & documentation

Mentoring junior staff

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking a Clinical Research Coordinator for a fully on-site role in Nebraska. You will gain exposure to multiple trials, manage site operations, and work closely with investigators and sponsors to ensure protocol adherence and patient safety.

The ideal candidate has hands-on clinical skills, experience with CTMS/eCRFs, and a track record of accurate regulatory documentation. This position offers a collaborative, fast-paced environment in a local SMO with global CRO backing.