On-Site Clinical Research Coordinator: Lead Multi‑Trial Studies

IQVIA; Rolla (MO); On-site; USD 66,000 - 111,000; Full time

Job summary

IQVIA, in partnership with Avacare SMO, seeks a Clinical Research Coordinator for an on-site role in Jefferson City, MO. You will support patient recruitment, consent and regulatory documentation, and help ensure trial conduct aligns with sponsor protocols.

This position offers exposure to multiple trials, hands-on responsibilities, and collaboration with investigators, sponsors, and monitors within a global CRO environment.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and lab specimen processing.
• Solid understanding of site operations and the drug development process.

Responsibilities

• Manage 2–6 trials of varying complexity and lead study coordination from start to finish.
• Mentor junior staff and contribute to internal training.
• Collaborate with investigators, sponsors, and monitors in a cross-functional team.
• Ensure accurate documentation and regulatory compliance across trials.

Skills

Clinical Skills

Site Operations Knowledge

CTMS

eCRFs

Microsoft Office

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA, in partnership with Avacare SMO, seeks a Clinical Research Coordinator for an on-site role in Jefferson City, MO. You will support patient recruitment, consent and regulatory documentation, and help ensure trial conduct aligns with sponsor protocols.

This position offers exposure to multiple trials, hands-on responsibilities, and collaboration with investigators, sponsors, and monitors within a global CRO environment.