Research Coordinator

IQVIA

Research Coordinator advocating for patient safety in clinical trials. Collaborating with clinical staff and documenting patient interactions to ensure compliance with protocols.

Posted 6/26/2026full-timeIrving • Texas, Virginia • 🇺🇸 United StatesMid-LevelSenior💰 $43,400 - $108,200 per yearWebsite

About the role

Key responsibilities & impact

Advocate for patient safety and protocol integrity
Assist with screening patients, scheduling, and overseeing study requirements
Attending teleconferences with sponsors and clinical research organizations
Collaborate with Principal Investigator and clinical staff for protocol compliance
Document patient encounters and ensure privacy and confidentiality of patients' source documents

Requirements

What you’ll need

5 or more years of experience
Current Texas or Virginia Registered Nursing License for RNs
Bachelor's degree required for non-RNs
Oncology clinical trial experience preferred
Research Coordination experience preferred

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work hours
Paid time off
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

patient safetyprotocol complianceclinical trial experienceresearch coordination

Soft Skills

advocacycollaborationcommunication

Certifications

Registered Nursing License