💼 About This Role

You'll travel with a team to clinical sites to conduct ophthalmic research using proprietary methodologies. Your core impact is ensuring subject safety and protocol adherence while performing data collection and clinical tasks. This role offers hands-on experience in a leading ophthalmic drug development firm.

🎯 What You'll Do

• Travel to research sites for clinical study visits
• Perform informed consent, vitals, and ophthalmic assessments
• Maintain study documents and enter data into electronic databases
• Collaborate with investigators and clinical project managers

📋 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 research coordinator experience
• Certified Ophthalmic Associate or Technician certification
• Phlebotomist (CPT) or EMT certification

🎁 Benefits & Perks

• ✈️ Travel opportunities to clinical sites
• 📚 Hands-on training and onboarding program

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

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

🚩 Heads Up

• 90% travel requirement may be excessive for some candidates
• Per-diem contract with inconsistent hours