On‑Site Senior CRC: Lead Multi‑Trial Coordination

IQVIA Inc; Jefferson City (MO); On-site; USD 44,000 - 111,000; Full time

Job summary

Avacare, an SMO backed by a global CRO, is seeking Clinical Research Coordinators to manage patient recruitment, consent, and regulatory documentation at our Jefferson City, MO site. You will gain exposure to multiple trials and work closely with investigators and monitors to ensure smooth study operations.

Ideal candidates have hands‑on clinical skills (vital signs, phlebotomy, ECGs) and experience with CTMS/eCRFs, plus proficiency in Microsoft Office.

Qualifications

• Hands-on clinical skills including vital signs, phlebotomy, ECGs, and lab specimens handling.
• Strong written and verbal communication with attention to detail and documentation.

Responsibilities

• Coordinate trials at the site, manage patient recruitment and informed consent, and ensure regulatory documentation.
• Support site audits, maintain study documentation, and assist investigators and monitors.

Skills

Communication skills

Time management

Clinical procedures

Tools

CTMS

eCRFs

Microsoft Office

Job description

Avacare, an SMO backed by a global CRO, is seeking Clinical Research Coordinators to manage patient recruitment, consent, and regulatory documentation at our Jefferson City, MO site. You will gain exposure to multiple trials and work closely with investigators and monitors to ensure smooth study operations.

Ideal candidates have hands‑on clinical skills (vital signs, phlebotomy, ECGs) and experience with CTMS/eCRFs, plus proficiency in Microsoft Office.