Planning, coordination, and management of clinical evaluation activities while ensuring compliance with regulatory requirements and internal quality standards Research, compilation, and analysis of clinical data from studies, tests, scientific literature, and post-market experience Preparation, review, and verification of clinical evaluation reports and related documentation to assess the safety and performance of MED-EL products in accordance with applicable regulations Continuous development and expansion of in-depth knowledge of the MED-EL product portfolio and its clinical application Close interdisciplinary collaboration with internal departments and external partners