Drug Safety Associate
Pubblicato il 20-08-2026 - Experteer Italy in Cusano Milanino
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
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