ppIn 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. /pulliannual leave entitlements /lilihealth insurance options /liliretirement planning offerings /liliGlobal Employee Assistance Programme LifeWorks /lililife assurance /liliflexible country-specific benefits /liliCollect and review adverse event reports from clinical trials and post-marketing sources /liliConduct initial assessment and coding of adverse events per procedures and regulatory guidelines /liliPrepare and submit expedited safety reports to regulatory authorities and investigators /liliAssist in development and maintenance of safety databases and tracking systems /liliCollaborate with cross-functional teams to ensure timely and accurate safety data reporting /liliBachelor's degree in a scientific or healthcare-related field /lili1-2 years of pharmacovigilance or drug safety experience in pharma/biotech preferred /liliKnowledge of pharmacovigilance regulations and guidelines (ICH, FDA, EMA) /liliStrong attention to detail and ability to work in a fast-paced environment /liliExcellent communication and organizational skills with cross-team collaboration and prioritization /li /ul /p #J-18808-Ljbffr

📌 Drug Safety Associate (Cusano Milanino)
🏢 Experteer Italy
📍 Cusano Milanino