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 entitlements
- health insurance options
- retirement planning offerings
- Global Employee Assistance Programme LifeWorks
- life assurance
- flexible country-specific benefits
- Collect and review adverse event reports from clinical trials and post-marketing sources
- Conduct initial assessment and coding of adverse events per procedures and regulatory guidelines




- Prepare and submit expedited safety reports to regulatory authorities and investigators
- Assist in development and maintenance of safety databases and tracking systems
- Collaborate with cross-functional teams to ensure timely and accurate safety data reporting
- Bachelor's degree in a scientific or healthcare-related field
- 1-2 years of pharmacovigilance or drug safety experience in pharma/biotech preferred
- Knowledge of pharmacovigilance regulations and guidelines (ICH, FDA, EMA)
- Strong attention to detail and ability to work in a fast-paced environment
- Excellent communication and organizational skills with cross-team collaboration and prioritization

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