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You will be updated with latest job alerts via emailAnalyze post-market surveillance data from global sources (e.g. MAUDE FAERS EUDAMED internal complaint databases) to detect safety signals and evaluate adverse event trends.
2. Organize and manage complex datasets using appropriate database systems and data structures.
3. Develop dashboards visualizations and summary reports for internal and external stakeholders including support for regulatory submissions.
4. Collaborate with cross-functional teams including safety physicians data scientists and regulatory experts to evaluate post-market safety data.
5. Maintain up-to-date knowledge of regulatory guidelines (e.g. FDA MDR ISO 14971) relevant to post-market safety and vigilance.
6. Contribute to the development and improvement of safety signal detection methodologies and tools.
7. Ensure adherence to data privacy ethics and compliance regulations in all analyses. Support and manage multiple projects simultaneously as per stakeholder requirements.
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Required Experience:
Senior IC
Full-Time