💼 About This Role

You'll travel to clinical research sites to conduct ophthalmic trials with proprietary methodologies. Your work ensures subject safety and protocol adherence while collecting and recording research data. This per-diem role offers hands-on experience in a leading ophthalmic contract research organization.

🎯 What You'll Do

• Travel to research sites for study visits
• Collect, record, and organize subject and research information
• Perform patient screening, recruitment, and enrollment
• Maintain study documents and ensure protocol compliance

📋 Requirements

• Bachelor's degree in Life Sciences OR 1 year clinical experience
• 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 like CPT or EMT

🎁 Benefits & Perks

• 🧑‍⚕️ Per-diem contract opportunity

📨 Hiring Process

Estimated timeline: 3-4 weeks · AI estimate

1. 13-week onboarding (virtual and in-person)· 3 weeks