• Medical assessment of the safety profile of the client's product range• Responsibility for evaluation of Adverse Events• Medical Review of aggregate reports• Preparing Clinical Expert Statements as per client requirement• Performing signal detection for client’s medicinal product• Preparation, evaluation and management of risk management plan.• Provide guidance and participation in the follow‐up of Adverse Events• Provide back‐up medical support on products/projects where required• Knowledge of local and national requirements for pharmacovigilance requirements.• Interact with staff at various levels and in various functional areas to resolve any issues that arise during reviews.• Contributing to the on‐going enhancement of Pharmacovigilance processes and writing Standard Operating Procedures.• Ensures that communication with all relevant people is of a high professional standard, and that records of both internal and external communication are maintained.• Ensuring compliance with local regulations and Company global pharmacovigilance requirements• Literature review for selection of ICSR and article of interest (for aggregate reports and signal detection).