💼 About This Role

You'll conduct ophthalmic clinical research at various sites, ensuring compliance with protocols and delivering an exceptional subject experience. This per-diem role requires extensive travel.

🎯 What You'll Do

• Travel to research sites for study visits and clinical conduct
• Perform informed consent, document medical history, take vitals, and dispense study drug
• Maintain source documentation, case report forms, and regulatory documents
• Screen, recruit, and enroll patients for clinical trials

📋 Requirements

• Bachelor's degree in Life Sciences OR 1 year of clinical experience
• Flexible schedule including weekend availability
• Ability to travel domestically up to 90% of the time
• Completion of 3-week onboarding training

✨ Nice to Have

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

🎁 Benefits & Perks

• 🩺 Per-diem contract opportunity

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Interview· 1 hour
3. 3Offer· 1 week