🛠 Tech Stack

💼 About This Role

You'll monitor clinical studies for Orca Bio, ensuring trials comply with protocols and regulations. Your work directly impacts patients fighting blood cancer by improving transplant outcomes. This role offers remote flexibility with travel for site visits.

🎯 What You'll Do

• Conduct interim monitoring visits and ISF review
• Review electronic medical records and perform source documentation verification
• Verify adverse events and concomitant medications for accurate reporting
• Author and submit monitoring visit reports within timelines

📋 Requirements

• BA/BS or equivalent degree
• 2+ years of CRA experience
• FDA and ICH/GCP regulations knowledge
• eTMF, EDC, CTMS system experience

✨ Nice to Have

• Therapeutic experience in oncology/hematology
• Prior sponsor-side CRA experience at a startup
• Experience with Trial Master File management

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical Interview· 60 min