💼 About This Role

You'll lead safety science and pharmacovigilance across Revolution Medicines' oncology portfolio, overseeing risk management and regulatory submissions. This role offers the chance to shape safety strategy for novel RAS-targeted therapies in a late-stage clinical company.

🎯 What You'll Do

• Perform medical review of ICSRs and routine safety data
• Lead safety surveillance strategy and signal detection
• Develop risk management plans and safety sections of regulatory documents
• Represent Safety Science in Health Authority meetings

📋 Requirements

• 10+ years drug development experience in pharma/biotech
• 6+ years Safety Science experience with medical review and surveillance
• Postgraduate qualification (MD, PharmD, PhD or equivalent)
• Experience with Regulatory Authority interactions (FDA, EMA)

✨ Nice to Have

• 4+ years Oncology clinical development experience
• BLA/MAA submission experience
• Global matrix leadership ability

🎁 Benefits & Perks

• 🏖️ Flexible PTO
• 🏥 Comprehensive health insurance
• 📈 Stock options
• 💼 401(k) matching
• 🎓 Professional development 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