Clinical Research Coordinator: Fast-Track Trials & Growth

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

Job summary

IQVIA Inc. is seeking Clinical Research Coordinators for on-site roles in Louisiana. You will recruit participants, obtain informed consent, and manage regulatory docs and site audits across trials. The role offers exposure to multiple therapeutic areas and collaboration with investigators, sponsors, and monitors.

Experience with CTMS, eCRFs, and MS Office is preferred. On-site travel between Covington and Kenner may be required as part of site management duties. IQVIA Inc.

Qualifications

• Hands-on clinical skills including vital signs, phlebotomy and ECGs.
• Experience with processing lab specimens.
• Solid understanding of site operations and drug development processes.

Responsibilities

• Recruit participants and obtain informed consent.
• Handle regulatory documentation for trials.
• Coordinate trial activities across sites and monitors.
• Manage study coordination from start to finish in multiple trials.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimens

CTMS

eCRFs

Microsoft Office

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA Inc. is seeking Clinical Research Coordinators for on-site roles in Louisiana. You will recruit participants, obtain informed consent, and manage regulatory docs and site audits across trials. The role offers exposure to multiple therapeutic areas and collaboration with investigators, sponsors, and monitors.

Experience with CTMS, eCRFs, and MS Office is preferred. On-site travel between Covington and Kenner may be required as part of site management duties. IQVIA Inc.