Clinical Research Coordinator: Multi‑Trial Lead

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

Benefits offered by this job

Equal opportunity employer

Job summary

IQVIA in Jefferson City, MO is seeking Clinical Research Coordinators (CRCs) to drive trial execution on-site. You will manage patient recruitment, informed consent, regulatory documents, and site audits across 2–6 trials, mentoring junior staff as needed.

The role emphasizes hands-on clinical procedures, CTMS/eCRF usage, and collaboration with investigators and monitors to ensure quality data and participant safety.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and lab specimen processing.
• Solid understanding of site operations and drug development process.
• Strong written and verbal communication with attention to detail and time management.
• Comfortable using CTMS, eCRFs, and MS Office tools.

Responsibilities

• Manage trials across multiple therapeutic areas from start to finish.
• Coordinate patient recruitment and informed consent processes.
• Ensure regulatory documentation and site audits are completed.
• Collaborate with investigators, sponsors, and monitors.

Skills

Clinical skills

Site operations

Communication & docs

Tech proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA in Jefferson City, MO is seeking Clinical Research Coordinators (CRCs) to drive trial execution on-site. You will manage patient recruitment, informed consent, regulatory documents, and site audits across 2–6 trials, mentoring junior staff as needed.

The role emphasizes hands-on clinical procedures, CTMS/eCRF usage, and collaboration with investigators and monitors to ensure quality data and participant safety.