💼 About This Role

You'll coordinate ophthalmic clinical trials, traveling to sites to administer technician-based tasks and ensure protocol compliance. Your work directly supports bringing new therapies to market. This role offers extensive travel and hands-on experience in a world-leading ophthalmic research firm.

🎯 What You'll Do

• Travel to clinical sites for study visits
• Collect, record, and organize subject data during visits
• Perform informed consent, vitals, and ophthalmic assessments
• Maintain study documents and ensure regulatory compliance

📋 Requirements

• Bachelor's degree in Life Sciences or 1 year clinical experience
• Willingness to travel domestically up to 90%
• Flexible schedule including weekend availability

✨ Nice to Have

• Previous experience as a research coordinator
• Certified Ophthalmic Associate or Technician certification
• Phlebotomy or EMT certification

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 60 min
3. 3Team interview· 45 min