Lead the end-to-end delivery of Real-World Evidence studies in Germany and France, managing timelines, budgets, and site coordination. Act as the primary operational contact for sponsors and coordinate cross-functional teams including medical, data, and legal departments.
You will act as a security partner for product and engineering teams, analyzing risks early and negotiating security requirements without blocking delivery. You will also manage vulnerability remediation, handle security incidents, and ensure compliance within a highly regulated healthcare environment.
You will build, operate, and secure data pipelines that transport healthcare data from production services to internal and external users. Additionally, you will manage infrastructure as code, ensure data quality through observability, and collaborate with product squads to industrialize data models.
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 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.
