In this role you will ensure the safety of investigational drugs and contribute to advancing innovative therapies. You work with your team and stakeholders to deliver high-quality pharmacovigilance outputs. You’ll handle adverse event data, support safety databases, and coordinate reporting to regulators. You join a culture focused on inclusion, collaboration, and delivering patient-focused safety outcomes. This position offers a meaningful impact in scaling safe, effective treatments for sponsors and patients.annual leave entitlementshealth insurance optionsretirement planning offeringsGlobal Employee Assistance Programme LifeWorkslife assuranceflexible country-specific benefitsCollect and review adverse event reports from clinical trials and post-marketing sourcesConduct initial assessment and coding of adverse events per procedures and regulatory guidelinesPrepare and submit expedited safety reports to regulatory authorities and investigatorsAssist in development and maintenance of safety databases and tracking systemsCollaborate with cross-functional teams to ensure timely and accurate safety data reportingBachelor's degree in a scientific or healthcare-related field1-2 years of pharmacovigilance or drug safety experience in pharma/biotech preferredKnowledge of pharmacovigilance regulations and guidelines (ICH, FDA, EMA)Strong attention to detail and ability to work in a fast-paced environmentExcellent communication and organizational skills with cross-team collaboration and prioritization
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📌 Drug Safety Associate (Cusano Milanino)
🏢 Experteer Italy
📍 Cusano Milanino