💼 About This Role

You'll provide safety science and pharmacovigilance support across the RevMed portfolio, including early and late phase clinical development. You will conduct medical safety surveillance and author safety documents like DSURs and RMPs. This role offers the opportunity to contribute to novel RAS-targeted oncology therapies.

🎯 What You'll Do

• Proactive medical safety surveillance of ongoing clinical trials
• Medical review of individual case safety reports
• Author aggregate safety reports and risk management plans
• Conduct signal detection and evaluation activities

📋 Requirements

• Postgraduate qualification (MD, PharmD, PhD/MSc in life sciences)
• 1+ years of drug development experience in pharmaceutical industry
• Detail-oriented with ability to prioritize tasks

✨ Nice to Have

• Understanding of pharmacovigilance and GVP/GCP
• Experience with individual case review
• Knowledge of clinical trial management and data review

🎁 Benefits & Perks

• 💰 Competitive base pay
• 📈 Robust equity awards
• 🏥 Strong benefits
• 📚 Significant learning and development opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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