Job Description

Clinical Research Coordinator II or III

📍 Peoria, AZ

💼 Full-Time | Onsite (Monday–Friday, 7am–4pm)

💰 Competitive Base Salary

About the Company

Our client is a leading multi-phase, multi-therapeutic clinical research organization dedicated to advancing medical innovation through high-quality clinical trials. Their mission is to deliver excellence in patient care, regulatory compliance, and clinical data integrity across a network of research and standard-of-care sites. Each location operates state-of-the-art facilities staffed by experienced physicians, research professionals, and patient outreach teams.

Position Overview

The Clinical Research Coordinator II or III is responsible for managing the day-to-day conduct of clinical trials under the direction of a Principal Investigator. This role involves protocol implementation, patient recruitment, data collection, and ensuring adherence to all regulatory and compliance standards.

Key Responsibilities

• Coordinate and implement assigned clinical research protocols in compliance with FDA regulations, GCP, and internal SOPs.
• Recruit, screen, and enroll study participants; ensure recruitment goals are achieved.
• Collect, record, and maintain accurate clinical data and source documentation.
• Prepare for and support study initiation, monitoring, and closeout visits.
• Manage investigational product accountability and maintain study supplies.
• Obtain informed consent and perform study procedures (phlebotomy, vitals, ECGs, lab processing, etc.).
• Monitor and document adverse events and serious adverse events per protocol.
• Maintain the clinical trial management system with real-time subject tracking and visit documentation.
• Assist with regulatory compliance, IRB submissions, and audit preparation.
• Train and mentor junior staff and serve as a liaison between investigators, site staff, and sponsors.

Qualifications

• Minimum 2 years of experience as a Clinical Research Coordinator (late-phase trials preferred).
• Associate’s or Bachelor’s degree in healthcare, life sciences, or related field (Master’s preferred).
• Strong understanding of GCP, ICH, and FDA regulatory standards.
• Excellent interpersonal, organizational, and data management skills.
• Proficiency with clinical trial management and EDC systems.
• GCP certification required; phlebotomy experience preferred.

Compensation & Benefits

• Competitive hourly pay
• Comprehensive health, dental, and vision insurance (HSA available with employer contribution)
• 401(k) with up to 6% employer match
• 3 weeks PTO + 5 days sick leave
• Short- and long-term disability
• Continuing education and tuition assistance
• Company-provided vehicle access for required travel

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