💼 About This Role

You'll lead global patient safety operations for clinical oncology programs at Revolution Medicines, overseeing PV CROs and ensuring regulatory compliance. You'll drive timely safety reporting across global regulatory authorities and investigators.

🎯 What You'll Do

• Oversee PV CRO execution of safety reporting in clinical studies
• Manage safety report submission to regulatory authorities and ethics committees
• Support authoring of clinical trial protocols and investigator brochures
• Collaborate on SAE reconciliation and query resolution activities

📋 Requirements

• Bachelor's degree in a healthcare field
• Minimum 5 years of pharmacovigilance operational experience
• Hands-on experience with CROs/vendors and external resource management
• Strong background in safety reporting regulatory compliance for global trials

✨ Nice to Have

• Master's degree or higher in a healthcare field
• 7+ years of relevant pharmacovigilance experience
• Experience with investigator-sponsored trials and business partnerships

🎁 Benefits & Perks

• 💰 Competitive cash compensation
• 📈 Robust equity awards
• 🏥 Strong benefits
• 🎓 Learning and development opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Panel interview· 60 min