You will support the intake, review, processing, and reporting of Individual Case Safety Reports (ICSRs) from clinical and post-marketed sources. You will help ensure compliance with Good Pharmacovigilance Practice (GVP), AstraZeneca procedures, and local health authority requirements.

The role also includes supporting regulatory authority queries, reconciliations, literature and database screening where required, quality and compliance activities, audit and inspection readiness, documentation and archiving, and collaboration with internal teams, service providers, and other external stakeholders.

We are seeking a candidate with:

• A degree in Pharmacy, Medicine, or a Science-related field


• Knowledge of pharmacovigilance and health authority regulations


• Strong attention to detail and problem-solving skills


• Excellent written and verbal commun...