DETAILS This position develops, documents and executes pre market and post market clinical evidence strategies for medical devices across product platforms. Works with cross functional teams and key stakeholders to execute on clinical evidence strategies for specific products/product families. For established products in the EU market, writes post market clinical follow up

OF MINIMUM QUALIFICATIONS Education and/or experience equivalent to a Bachelor's Degree in a technical field such as the biological, physical, engineering, or material science disciplines. Seven years of relevant regulatory experience. Demonstrated or verifiable experience with authoring regulatory submissions and interacting with reviewers. Demonstrated knowledge of globa