💼 About This Role

You'll administer technician-based tasks during ophthalmic clinical trial visits, ensuring protocol compliance and an exceptional subject experience. Your work directly supports the world's leading ophthalmic development firm in bringing new therapies to market.

🎯 What You'll Do

• Collect, record, and organize subject and research information during study visits
• Perform the Informed Consent process and document medical history
• Take vitals, scribe for medical staff, and dispense study drug
• Enter data into electronic database and resolve data queries

📋 Requirements

• Bachelor's degree in Life Sciences OR 1-year experience in a clinical setting
• Willingness to travel domestically up to 90% of the time
• Flexible schedule including weekend availability

✨ Nice to Have

• Previous experience as a research coordinator
• Certified Ophthalmic Associate or Technician certification
• Medical certifications (CPT, EMT) preferred

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Technical Interview· 60 min
3. 3Offer· 30 min