Experteer Overview
In this role you support global pharmacovigilance activities for a broad portfolio of products, ensuring patient safety and regulatory compliance. You will collaborate with cross-functional teams to manage post-marketing safety surveillance and contribute to safety reporting. The position offers international exposure and the chance to influence integral safety practices. You join a collaborative environment that emphasizes professional growth and meaningful impact on patients and healthcare professionals.
Compensaciones / Beneficios
• Perform routine global pharmacovigilance activities: aggregate reporting, signal detection, literature monitoring, and risk management
• Lead and coordinate preparation and review of aggregate safety reports for quality, accuracy, and regulatory compliance
• Provide scientific oversight of external pharmacovigilance service providers
• Support regulatory submissions, maintenance of marketing authorisations, and responses to health authority requests
• Contribute as SME to upgrades/improvements of PV databases and tools
• Prepare and maintain departmental quality documents and support process improvements
Responsabilidades
• Five+ years of experience in life sciences with significant pharmacovigilance and post-marketing safety exposure at global or HQ level
• Strong knowledge of post-marketing PV regulations for medicinal products and awareness of cosmetics regulations
• Extensive experience in aggregate reporting, risk management, and signal detection
• Experience collaborating with external providers, local affiliates, and cross-functional stakeholders
• Strong analytical skills, attention to detail, and ability to manage multiple activities and deadlines
• Excellent written and spoken English
Requisitos principales
• international and collaborative working environment
• opportunities for professional development
• contribution to global pharmacovigilance activities
• meaningful impact on patient safety