On-Site Clinical Research Coordinator – Multi-Trial Focus

IQVIA Argentina; Kenner (LA); On-site; USD 38,000 - 95,000; Full time

Job summary

Avacare, an SMO, seeks a Clinical Research Coordinator to manage patient recruitment, informed consent, and regulatory documentation across multiple trials. The role requires hands-on clinical procedures and collaboration with investigators and monitors.

Ideal candidates have CTMS/eCRF familiarity, strong communication, and timely documentation. Eligible for on-site work in Louisiana with travel between Covington and Kenner.

Qualifications

• Hands-on experience collecting vital signs, phlebotomy, ECGs, and lab processing.
• Must have experience with pediatric blood draws.
• Professional ability to document accurately and manage trial records.

Responsibilities

• Coordinate 2–6 trials with varying complexity and lead study activities.
• Recruit patients and obtain informed consent.
• Maintain regulatory documentation and support site audits.

Skills

Clinical Skills

Communication

Documentation

Time Management

Tools

CTMS

eCRFs

Microsoft Office

Job description

Avacare, an SMO, seeks a Clinical Research Coordinator to manage patient recruitment, informed consent, and regulatory documentation across multiple trials. The role requires hands-on clinical procedures and collaboration with investigators and monitors.

Ideal candidates have CTMS/eCRF familiarity, strong communication, and timely documentation. Eligible for on-site work in Louisiana with travel between Covington and Kenner.