Onsite Clinical Research Coordinator - Multi-Trial Lead

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

Job summary

IQVIA in Covington/Kenner area is seeking a Clinical Research Coordinator for an on-site role requiring travel from Covington LA to Kenner LA. You will support multiple trials, manage patient recruitment, informed consent, and regulatory documentation while coordinating study activities.

Experience in CTMS/eCRFs and Microsoft Office is essential. The role offers exposure to diverse trials, collaboration with investigators, sponsors, and monitors, and potential growth within a global CRO.

Qualifications

• Hands‑on experience obtaining vital signs, performing phlebotomy, ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• Proficient in pediatric phlebotomy, including infants.

Responsibilities

• Manage patient recruitment and informed consent processes across trials.
• Maintain regulatory documentation and trial master files.
• Coordinate study activities from start to finish and communicate with investigators.
• Prepare for site audits and ensure protocol compliance.

Skills

Clinical Skills

Pediatric phlebotomy

Communication

Documentation

Time management

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA in Covington/Kenner area is seeking a Clinical Research Coordinator for an on-site role requiring travel from Covington LA to Kenner LA. You will support multiple trials, manage patient recruitment, informed consent, and regulatory documentation while coordinating study activities.

Experience in CTMS/eCRFs and Microsoft Office is essential. The role offers exposure to diverse trials, collaboration with investigators, sponsors, and monitors, and potential growth within a global CRO.