💼 About This Role

You'll build close relationships with subjects during clinical trial visits, traveling to sites across the US to conduct ophthalmic research using proprietary methodologies. Your core impact is ensuring protocol compliance and exceptional subject experiences.

🎯 What You'll Do

• Travel to clinical sites and perform study visits
• Record and organize subject and research data
• Perform screening, recruitment, and enrollment
• Ensure protocol compliance and data integrity

📋 Requirements

• Bachelor's degree in Life Sciences
• 1 year experience in a clinical setting
• Flexible schedule including weekends
• Willingness to travel up to 90%

✨ Nice to Have

• Research coordinator experience
• COA/COT certification
• Phlebotomy or EMT certification

🎁 Benefits & Perks

• 🏖️ Per-diem contract with flexible hours
• 🚗 Travel to clinical sites covered

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 60 min
3. 3Onboarding training· 3 weeks