🛠 Tech Stack

💼 About This Role

You'll lead adverse event processing and safety data analysis for a regulated pharmaceutical environment, ensuring compliance with global pharmacovigilance requirements and contributing directly to patient safety.

🎯 What You'll Do

• Lead adverse event report collection and evaluation
• Analyze safety data to identify potential signals
• Prepare and submit periodic safety update reports
• Provide mentorship to junior pharmacovigilance staff

📋 Requirements

• Bachelor's degree in life sciences or related field
• Strong experience in pharmacovigilance within pharma
• Solid understanding of global pharmacovigilance regulations
• Proven experience in adverse event reporting and signal detection

✨ Nice to Have

• Advanced degree in life sciences or pharmacy
• Experience with pharmacovigilance databases
• Regulatory audit or inspection experience

🎁 Benefits & Perks

• 🏖️ Competitive compensation package aligned with industry
• 🏥 Comprehensive health insurance for employees and families
• 📈 Retirement savings and pension planning options
• 🌍 Global employee assistance program with 24/7 support
• 📚 Professional development and career growth opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Technical Interview· 60 min
3. 3Hiring Manager Interview· 45 min