💼 About This Role

You'll lead early clinical development for RAS-addicted cancer therapies at a late-stage oncology company. Your work will drive phase 1 trials and shape the pipeline from early studies to regulatory submissions.

🎯 What You'll Do

• Develop clinical development plans for RAS(ON) inhibitors
• Design and execute phase 1 clinical trials
• Lead cross-functional teams of clinical development professionals
• Manage regulatory interactions with FDA and EMA

📋 Requirements

• MD or PhD with 13+ years in pharma/biotech
• Experience designing and conducting phase 1 clinical trials
• Expertise in GCP and FDA/EMA regulations
• Track record of authoring clinical development strategies

✨ Nice to Have

• Experience submitting NDA/BLA/MAA to health authorities
• Experience with phase IV drug development
• Leadership in regulatory documentation for labels

🎁 Benefits & Perks

• 🏥 Health insurance
• 💰 Competitive compensation
• 🚀 Stock options
• 🏖️ PTO
• 📚 Continuing education support

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 60 min
3. 3Panel interview· 90 min