Clinical Research Coordinator - Diverse Trials & On-Site Growth

IQVIA Argentina; Gilbert (AZ); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA is seeking a Clinical Research Coordinator for an on-site role in Gilbert, AZ. You will manage patient recruitment, informed consent, and regulatory documentation while coordinating trial activities across multiple studies in a fast-paced, collaborative environment.

You will gain experience across therapeutic areas, interact with investigators and sponsors, and contribute to site audits. CTMS/eCRFs and MS Office skills are essential, with growth opportunities within a global CRO.

Qualifications

• Hands-on experience with vital signs, phlebotomy, ECGs, and lab specimens.
• Solid understanding of site operations and the drug development process.
• Strong written and verbal communication skills with attention to detail.

Responsibilities

• Manage patient recruitment and informed consent processes.
• Oversee regulatory documentation and site audits.
• Coordinate trial activities across 2–6 studies.
• Collaborate with investigators, sponsors, and monitors.
• Mentor junior staff and contribute to internal training.

Skills

Clinical skills

Site operations

Communication & documentation

Technical proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking a Clinical Research Coordinator for an on-site role in Gilbert, AZ. You will manage patient recruitment, informed consent, and regulatory documentation while coordinating trial activities across multiple studies in a fast-paced, collaborative environment.

You will gain experience across therapeutic areas, interact with investigators and sponsors, and contribute to site audits. CTMS/eCRFs and MS Office skills are essential, with growth opportunities within a global CRO.