You will ensure the compliance and robustness of medical software throughout its lifecycle by integrating quality requirements into the development process. You will also maintain the Quality Management System, manage technical documentation, and oversee post-market surveillance and CAPA activities.
You will develop and execute statistical analysis plans for real-world evidence and medical affairs studies. This involves programming analyses, ensuring data quality, and communicating complex results to cross-functional teams.
You will design and deliver machine learning models on real-world patient health data to support Medical Affairs studies and product development. You will also build and maintain automated scoring pipelines while partnering with cross-functional teams to ensure actionable clinical insights.
You will act as the primary product owner and design lead for the US market, managing the product backlog and conducting discovery cycles with clinical partners. You are responsible for shipping end-to-end features that integrate with US healthcare systems like EHRs and CMS billing workflows.
