💼 About This Role

You'll manage day-to-day operations of Phase 1-3 clinical trials at a late-stage biotech. You'll oversee CROs, vendors, and study execution to ensure timelines, budgets, and quality. This contract role offers remote flexibility with a company advancing gene therapies for retinal and pulmonary diseases.

🎯 What You'll Do

• Serve as primary contact for protocol execution and CRO oversight
• Lead cross-functional study execution team to meet milestones
• Manage trial budgets, contracts, and vendor selection
• Ensure TMF maintenance and audit-readiness

📋 Requirements

• 6+ years clinical research experience in biotech
• 2+ years direct clinical trial management
• Knowledge of GCP, ICH guidelines and regulations
• Experience with CRO oversight and vendor management

✨ Nice to Have

• Experience in ophthalmology or gene therapy trials
• Prior contract role experience
• Site management and monitoring background

🎁 Benefits & Perks

• 🏖️ Remote work flexibility
• 💰 Competitive contract rate
• 📈 Career growth in late-stage biotech
• 🏥 Health benefits (if applicable per contract)

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Phone Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Panel Interview· 1 hour

🚩 Heads Up

• Contract role without clear benefits stated
• Potentially high workload with multiple trial oversight