Clinical Research Coordinator: Lead Multi-Trial Coordination

IQVIA LLC; Kansas City (MO); On-site; USD 38,000 - 95,000; Full time

Benefits offered by this job

Incentives

Health benefits

Job summary

IQVIA is seeking a Clinical Research Coordinator to join Avacare, a dynamic SMO that provides CRCs with exposure to diverse trials and hands-on responsibilities. You will recruit patients, obtain informed consent, manage regulatory documentation, and support site audits within a collaborative team.

Ideal candidates have 1–3 years CRC experience (CRC II up to 3 years), hands-on skills in vital signs, phlebotomy, ECGs, CTMS/eCRFs, and proficiency with Microsoft Office.

Qualifications

• CRC I: 1–3 years in clinical research at a site with participants.
• CRC II: 3+ years as a CRC at a clinical investigative site.
• Hands-on skills: vital signs, phlebotomy, ECGs, lab processing.
• CTMS/eCRFs and MS Office proficiency required.

Responsibilities

• Recruit patients and obtain informed consent.
• Manage regulatory documentation and site approvals.
• Coordinate trial activities across sites and monitors.
• Support audits and close-out activities.

Skills

Clinical skills

Site operations

Communication

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking a Clinical Research Coordinator to join Avacare, a dynamic SMO that provides CRCs with exposure to diverse trials and hands-on responsibilities. You will recruit patients, obtain informed consent, manage regulatory documentation, and support site audits within a collaborative team.

Ideal candidates have 1–3 years CRC experience (CRC II up to 3 years), hands-on skills in vital signs, phlebotomy, ECGs, CTMS/eCRFs, and proficiency with Microsoft Office.