↳A master-s degree or PhD in health sciences, audiology, medicine, biomedical engineering, psychology, life sciences or a related field.
↳Experience working with clinical studies or investigations, for example conducting, coordinating or monitoring clinical studies.
↳Experience working with clinical data and the ability to critically interpret clinical study results, scientific publications and relevant statistical analyses.
↳Experience conducting scientific literature searches using databases such as PubMed, Cochrane or Embase, as well as critically appraising and summarizing the identified evidence.
↳Knowledge of relevant clinical and medical-device regulations and standards, such as EU MDR, FDA requirements, GCP or ISO 14155.
↳Strong analytical skills and attention to detail.
↳Ability to work independently, take ownership and manage responsibilities and deadlines effectively.
↳A collaborative, self-motivated approach and the ability to communicate openly and effectively across interdisciplinary teams.
↳Fluency in English is required; knowledge of German would be an advantage.
