Pharmacovigilance Scientist 2
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In this role, you lead signal detection and literature surveillance for marketed and investigational products, ensuring timely identification of safety signals. You author and QC aggregate reports such as PBRERs/PSURs, DSURs, and ACOs, and respond to regulatory inquiries. You may serve as molecule lead, owning deliverables and coordinating across cross-functional teams to maintain quality and compliance. You drive end-to-end signal management from detection to inclusion in reports, partnering with customers and service providers. This is a hands-on, impact-driven position in a global pharmacovigilance setting with scope for leadership and process improvement.
Compensaciones / Beneficios
• Lead signal detection activities and literature surveillance for safety signals
• Author and QC aggregate safety reports (PBRERs/PSURs, DSURs, ACOs)
• Prepare responses to regulatory inquiries
• Own molecule deliverables and ensure KPI-compliant delivery
• Coordinate signaling strategies and track signals from detection to reporting
• Liaise with portfolio scientists and cross-functional stakeholders
• Oversee team workload distribution and ensure timely molecule deliverables
• Maintain in-depth knowledge of the molecule and disease area
• Participate in audits and ensure SOP compliance
• Conduct lessons learned to Cascade customer information to xghoner teams
Responsabilidades
• Life science graduate/post-graduate, pharmacy, nursing or healthcare-related qualification or PV experience
• 4-6 years of pharmacovigilance experience including hands-on drug safety, aggregate reports, signal detection/signal management
• Excellent written and verbal communication skills
• Team-oriented with ability to collaborate across functions
• English fluent (spoken and written)
Requisitos principales
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