Clinical Research Coordinator — Multi-Trial Lead (Onsite)

Regulatory Jobs; Covington (LA); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA in the United States is seeking a Clinical Research Coordinator (CRC) for an on-site role in Covington, LA, with travel to Kenner, LA. You will support multiple trials, manage patient recruitment, informed consent, and regulatory documentation in a collaborative SMO setting.

Ideal candidates bring hands-on clinical skills, knowledge of CTMS/eCRFs, and strong communication. You’ll coordinate site activities, support monitors, and contribute to audits, with growth opportunities in clinical

Qualifications

• H hands-on vital signs collection and phlebotomy.
• ECG performance and lab specimen processing.
• Solid knowledge of site operations and drug development.
• Pediatric phlebotomy experience, including infants.
• CRC I/CRC II experience with participants.
• Strong written and verbal communication, time management.
• Proficient with CTMS, eCRFs and MS Office.

Responsibilities

• Recruit participants and obtain informed consent.
• Regulatory documentation and site audits.
• Coordinate trial activities across multiple protocols.

Skills

Vital signs

Phlebotomy

ECG

Lab specimens

Site operations

CTMS

eCRFs

Microsoft Office

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA in the United States is seeking a Clinical Research Coordinator (CRC) for an on-site role in Covington, LA, with travel to Kenner, LA. You will support multiple trials, manage patient recruitment, informed consent, and regulatory documentation in a collaborative SMO setting.

Ideal candidates bring hands-on clinical skills, knowledge of CTMS/eCRFs, and strong communication. You’ll coordinate site activities, support monitors, and contribute to audits, with growth opportunities in clinical