On-Site Clinical Research Coordinator — Lead Trials & Grow

IQVIA LLC; Tempe (AZ); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA is hiring a Clinical Research Coordinator at our Tempe, AZ site. This on-site role offers exposure across multiple trials, with hands-on responsibilities in patient recruitment, informed consent, regulatory documentation and site audits.

You will work closely with investigators, sponsors, and monitors to support high-quality trial conduct. You will manage vital signs, phlebotomy, ECGs and lab sample handling while using CTMS and eCRFs, alongside MS Office.

Qualifications

• Hands-on clinical skills including vitals, phlebotomy, ECGs and lab processing.
• Familiarity with CTMS, eCRFs and MS Office tools.
• Strong written and verbal communication with attention to detail.

Responsibilities

• Manage patient recruitment and obtain informed consent.
• Oversee regulatory documentation and site audits.
• Handle data entry and documentation using CTMS/eCRFs and MS Office.
• Support multiple trials across therapeutic areas from start to finish.

Skills

Clinical Skills

Site Operations Knowledge

Communication & Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is hiring a Clinical Research Coordinator at our Tempe, AZ site. This on-site role offers exposure across multiple trials, with hands-on responsibilities in patient recruitment, informed consent, regulatory documentation and site audits.

You will work closely with investigators, sponsors, and monitors to support high-quality trial conduct. You will manage vital signs, phlebotomy, ECGs and lab sample handling while using CTMS and eCRFs, alongside MS Office.