Clinical Research Coordinator: Lead Multi-Trial Studies

IQVIA LLC

Gilbert (AZ)

On-site

USD 38,000 - 95,000

Full time

14 days+
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Job summary

Avacare, an SMO, is seeking Clinical Research Coordinators for a fully on-site role in Gilbert, AZ. You will gain exposure to multiple therapeutic areas, manage protocols, and own trial activities from recruitment and informed consent to regulatory documentation and site audits.

Work with investigators, sponsors, and monitors, mentor junior staff, and contribute to internal training. Develop hands-on CRC skills across trials, including vital signs, phlebotomy, ECGs, and data capture in CTMS and

Qualifications

  • Hands-on clinical skills required and demonstrated in trial settings.
  • Experience as CRC I/II at an investigative site.
  • Strong documentation and time management abilities.
  • Ability to manage multiple trials and regulatory tasks.

Responsibilities

  • Recruit patients and obtain informed consent in a timely, compliant manner.
  • Perform vital signs, phlebotomy, ECGs and handle lab specimens.
  • Maintain regulatory documents and prepare site for audits.
  • Coordinate study activities with investigators, sponsors and monitors.

Skills

Vital signs
Phlebotomy
ECGs
Lab specimen processing
Site operations
Study coordination
Communication
Documentation

Tools

CTMS
eCRFs
Microsoft Office

Job description

Avacare, an SMO, is seeking Clinical Research Coordinators for a fully on-site role in Gilbert, AZ. You will gain exposure to multiple therapeutic areas, manage protocols, and own trial activities from recruitment and informed consent to regulatory documentation and site audits.

Work with investigators, sponsors, and monitors, mentor junior staff, and contribute to internal training. Develop hands-on CRC skills across trials, including vital signs, phlebotomy, ECGs, and data capture in CTMS and

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