Clinical Research Coordinator - Diverse Trials & Growth

IQVIA; Rolla (MO); On-site; USD 44,000 - 111,000; Full time

Job summary

IQVIA, Jefferson City, MO, is seeking a Clinical Research Coordinator for an on-site role supporting multiple trials. You’ll manage patient recruitment, informed consent, and regulatory documentation, gaining hands-on experience across therapeutic areas.

Collaborate with investigators, sponsors, and monitors; coordinate visits, collect data in CTMS/eCRFs, and help ensure trial quality and compliance. This fast-paced, team-focused position offers growth within a globally connected CRO.

Qualifications

• Hands-on clinical skills including vitals, phlebotomy, ECGs, and lab specimen handling.
• Strong knowledge of site operations and drug development processes.
• CRC experience at a clinical investigative site (1–3 years for CRC I; 3+ years for CRC II).

Responsibilities

• Coordinate trials from patient recruitment to regulatory documentation.
• Mentor junior staff and contribute to internal training.
• Collaborate with investigators, sponsors, and monitors; ensure data quality.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimens

CTMS

eCRFs

Microsoft Office

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA, Jefferson City, MO, is seeking a Clinical Research Coordinator for an on-site role supporting multiple trials. You’ll manage patient recruitment, informed consent, and regulatory documentation, gaining hands-on experience across therapeutic areas.

Collaborate with investigators, sponsors, and monitors; coordinate visits, collect data in CTMS/eCRFs, and help ensure trial quality and compliance. This fast-paced, team-focused position offers growth within a globally connected CRO.