💼 About This Role

You'll coordinate clinical trials at a leading liver health research network. You'll manage participant recruitment, data entry, and regulatory compliance. This temporary role offers a path to permanent employment.

🎯 What You'll Do

• Screen and enroll participants per study protocol
• Collect and process blood and biospecimens
• Enter data into EDC systems and resolve queries
• Prepare and maintain regulatory documents and IRB submissions

📋 Requirements

• 3 years of clinical research experience
• High school diploma or GED
• GCP certification (can be obtained upon hire)
• Authorization to work in the U.S. (no visa sponsorship)

✨ Nice to Have

• Bachelor's degree in health sciences or related field
• IATA certification
• Phlebotomy experience

🎁 Benefits & Perks

• 💰 $35/hour pay rate
• 📅 4-month contract with potential for permanent role
• ⏰ Overtime eligible

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Recruiter call· 30 min
2. 2Hiring manager interview· 45 min
3. 3Offer· 1 week