🛠 Tech Stack

💼 About This Role

You'll support a Phase 3 clinical trial at a leading biotechnology company, acting as a key liaison between the sponsor, clinical sites, and CRO partners. Your work will directly impact the timely execution of study milestones and regulatory compliance. This contract role offers hands-on experience in ophthalmology trials.

🎯 What You'll Do

• Serve as primary point of contact for assigned clinical sites and CRO monitors
• Review monitoring visit reports and follow up on action items
• Maintain tracking tools for site status, enrollment, and essential documents
• Collect, review, and track site regulatory documents for TMF compliance

📋 Requirements

• 1-2 years of clinical trial experience in sponsor or CRO environment
• Working knowledge of ICH GCP guidelines
• Experience with TMF/eTMF systems (Veeva Vault preferred)

✨ Nice to Have

• Phase 3 clinical trial experience
• Ophthalmology experience

🎁 Benefits & Perks

• 💵 Hourly rate: $38.00 - $52.00/hour
• 🏠 Remote work flexibility
• 📅 Contract position with potential for extension
• 🧬 Work on cutting-edge gene therapy for retinal diseases

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Application Review· 1-2 weeks
2. 2Phone Screen with Recruiter· 30-45 min
3. 3Hiring Manager Interview· 1 hour

🚩 Heads Up

• Mentions contract but role responsibilities are typical for permanent; ambiguous job security