Manager - Drug Safety Risk Management - Consulting Firm

- Provide medical oversight for clinical studies

- Preparation and review of study documents e.g. Protocol, Investigator brochure, Safety Management Plan, CRFs, Informed consent forms, Clinical Study Report and other relevant study related documents

- Medical review of clinical trial data, final approver, for any medical/safety query closure

- Preparation and review of relevant SOPs

- Provide appropriate training study team

- Any other clinical research and pharmacovigilance activities within department