💼 About This Role

You'll lead clinical development of rapid-acting neuroplastogen for PTSD, providing medical oversight of Phase 3 trials. You'll shape regulatory strategy and build KOL relationships in a fast-growing biotech.

🎯 What You'll Do

• Develop and execute clinical trial protocols with scientific rigor
• Serve as medical monitor overseeing patient safety and data quality
• Analyze and interpret clinical data to guide development strategy
• Author key clinical documents (protocols, IB, CSR, regulatory submissions)

📋 Requirements

• MD or equivalent degree
• 5+ years drug development experience in pharma
• 2+ years in neuroscience indications
• Board-certified psychiatrist preferred

✨ Nice to Have

• Experience with FDA/EMA regulatory interactions
• Experience in a small, fast-paced team

🎁 Benefits & Perks

• 💰 Competitive cash and equity compensation
• 🏥 Medical, dental, vision insurance
• 🏖️ Unlimited vacation and sick time
• 🏦 401k plan