💼 About This Role

You'll join Ora's Global Project Delivery team to conduct ophthalmic clinical trials at various sites. Your core impact is ensuring subject safety and protocol adherence while collecting and organizing research data. You'll travel extensively with a team to perform technician-based tasks at clinical sites.

🎯 What You'll Do

• Travel to research sites as assigned for study visits
• Perform informed consent process and document medical history
• Collect and organize subject data and research information
• Maintain study documents and ensure protocol compliance

📋 Requirements

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

✨ Nice to Have

• Previous research coordinator experience
• Certified Ophthalmic Assistant or Technician certification
• Phlebotomy or EMT certification

🎁 Benefits & Perks

• 🏖️ Per diem contract with flexible schedule

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Onboarding Training· 3 weeks

🚩 Heads Up

• Up to 90% travel may be excessive for entry-level role
• Per diem contract offers limited job security