💼 About This Role

You'll lead strategic oversight of aggregate reporting, risk management, and surveillance operations for a global CRO serving top pharma and biotech clients. Your core impact is ensuring regulatory compliance and quality across all safety reports. This role offers the chance to shape a growing pharmacovigilance practice and drive innovation in safety surveillance.

🎯 What You'll Do

• Oversee end-to-end production of aggregate safety reports (PBRER, DSUR, RMP).
• Lead and mentor a team of safety scientists and report writers.
• Establish optimization processes for quality, compliance, and efficiency.
• Act as primary client contact for key sponsor relationships.

📋 Requirements

• 15+ years in pharmacovigilance or drug safety aggregate reporting.
• Graduate or post-graduate degree in Life Sciences or Healthcare.
• Expertise in global PV regulations (ICH, GVP, FDA, EU MDR).
• Proven experience leading team management and client engagement.

✨ Nice to Have

• Experience in medical device or cosmetics safety.
• Familiarity with safety databases and automation tools.
• Knowledge of business development and proposal writing.

🎁 Benefits & Perks

• 🏖️ Flexible work arrangements
• 📈 Career development programs
• 🌍 Global exposure with international teams

📨 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