🛠 Tech Stack

💼 About This Role

You'll coordinate and manage clinical research activities for late-phase trials at Arizona Liver Health, ensuring compliance with FDA, GCP, and SOPs. Your work will directly impact patient safety and data integrity across multiple studies. This role offers hands-on patient interaction and opportunities to mentor junior staff.

🎯 What You'll Do

• Recruit and screen potential study participants
• Collect and record clinical research data
• Maintain study files and study medication accountability
• Coordinate site activities during audits and inspections

📋 Requirements

• 2 years experience as Clinical Research Coordinator for late phase trials
• GCP training and knowledge of FDA CFR
• Phlebotomy and basic lab test skills
• ECG administration and vital signs assessment

✨ Nice to Have

• Experience with electronic data capture systems
• Previous supervisory experience

🎁 Benefits & Perks

• 💰 Competitive hourly rate $27.50-$36/hr
• 📅 Set schedule Monday-Friday, 7am-4pm
• 🏥 Full-time, non-exempt with benefits

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3On-site Interview· 1 hour

🚩 Heads Up

• No mention of benefits beyond pay and schedule
• Broad range of duties may indicate role overload