Clinical Research Coordinator - Lead Multi-Trial Site Ops

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

Job summary

IQVIA is seeking a fully on-site Clinical Research Coordinator in Scottsdale, Arizona. You will gain exposure across multiple trials, manage procedures, and coordinate study activities from recruitment to regulatory documentation.

Ideal candidates have hands-on clinical skills and experience with CTMS/eCRFs, plus strong communication and time management. This role offers growth within a global CRO network and collaborative culture.

Qualifications

• Hands-on skills: vital signs, phlebotomy, ECGs, lab specimen processing.
• Solid understanding of site operations and drug development processes.
• CRC progression: CRC I 1–3 years; CRC II 3+ years at a clinical site.

Responsibilities

• Coordinate 2–6 trials of varying complexity, lead study coordination from start to finish.
• Collaborate with investigators, sponsors, and monitors; mentor junior staff.
• Support regulatory documentation and site audits; ensure compliance and data integrity.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimen processing

Site operations

Communication

Documentation

Time management

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking a fully on-site Clinical Research Coordinator in Scottsdale, Arizona. You will gain exposure across multiple trials, manage procedures, and coordinate study activities from recruitment to regulatory documentation.

Ideal candidates have hands-on clinical skills and experience with CTMS/eCRFs, plus strong communication and time management. This role offers growth within a global CRO network and collaborative culture.