Pharmacovigilance Associate - VIE Contract

Pharmacovigilance Associate - VIE Contract • Location: Singapore, Singapore • Target start date: 01/03/2027 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address. About the job As Pharmacovigilance Associate VIE within our Patient Safety & Pharmacovigilance team, you’ll assist with pharmacovigilance responsibilities ensuring corporate and regulatory requirements are met for all Sanofi products in Singapore. You will support the Country Safety Head in the intake, processing and reporting of local Individual Case Safety Reports (ICSRs) in full compliance with local and global safety regulations as required by local Health Authorities. Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. Ready to get started? About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main responsibilities: • Collect information on adverse events (AEs) for all Sanofi products • Assess and evaluate information received against minimal reporting criteria, internal and regulatory guidelines. • In collaboration with external vendor, ensure processing of local individual case safety reports (ICSRs) is completed in accordance with local and corporate policies and standard operating procedures (SOPs). • Assist the Country Safety Head in providing education and training on safety topics within Sanofi Singapore, including documentation of attendees and topics covered (new employee training, PV awareness training, training of service providers). • Perform root cause analysis (RCA) and implement appropriate corrective actions/ preventative actions (CAPAs) when required. • Review of digital and market research projects to ensure compliance with PV requirements. • Support the Country Safety Head in signal management activities including documentation of Significant Safety Issues (SSIs). About you Experience: • Knowledge of the European Union’s Good Pharmacovigilance Practices (GVP) regulations and pharmacovigilance guidelines will be an asset. Soft and technical skills: • Good understanding of medical terminology. • Excellent verbal and written communication skills. • Attention to detail. • Works well independently and as part of a team. • Microsoft Office skill. • Presentation skills. Education: • Degree in pharmacy, medicine, science or related discipline. Languages: • Fluent English (written and verbal). Why choose us? • Be part of a pioneering biopharma company where patient insights shape drug development. • Work at the forefront of AI-powered science that accelerates discovery and improves outcomes. • Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams. • Help improve the lives of millions of people globally by making drug development quicker and more effective. • Enjoy opportunities to collabora