💼 About This Role

You'll provide safety science and pharmacovigilance support across the RevMed portfolio, including early and late phase development activities. You'll be responsible for safety oversight of clinical studies and authoring key safety documents. This role offers the chance to contribute to novel targeted therapies for RAS-addicted cancers.

🎯 What You'll Do

• Perform medical safety surveillance of ongoing clinical trials
• Prepare and present safety data summaries to stakeholders
• Medical review of Individual Case Safety Reports (ICSRs)
• Contribute to regulatory filings and responses to safety queries

📋 Requirements

• Postgraduate qualification (MD, PharmD, PhD, MSc in Life Sciences)
• 3+ years drug development experience with at least 1 year in drug safety
• Understanding of safety and pharmacovigilance (GVP, GCP, risk management)
• Proven relationship-building with internal and external partners

✨ Nice to Have

• Experience with oncology products
• Signal detection and evaluation experience
• Prior involvement in regulatory submissions (NDAs, BLAs)

🎁 Benefits & Perks

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

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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