Jurist / Syndikus Regulatory Governance & BaFin Office (m / w / d)

To support our research team, we are looking for someone like you.

Sonova and our brands offer very good perspectives and career opportunities.

We foster an atmosphere of mutual trust in a highly motivated team.

This position offers a permanent contract with mobile working options.

You will help improve the quality of life for millions of people with hearing loss.

Main tasks and responsibilities:

• Design, implement, and conduct clinical studies to investigate new technologies in cochlear implant users, particularly in the audiological domains.
• Define and supervise EU-wide collaborative research projects with external partners.
• Design and conduct clinical activities to support regulatory clinical requirements from MDR (CER, PMCF).
• Present at scientific conferences and prepare scientific publications.
• Provide scientific information for product launch support and marketing purposes.

Your profile:

• University Degree in Physics, Engineering, Audiology, or equivalent fields.
• At least two years of experience in clinical research in a medical field, ideally in the auditory implant area.
• Willingness to travel internationally (20-30%).
• Knowledge of medical terminology and clinical study design, expertise with regulatory compliance guidelines (MDR), and familiarity with statistical techniques for data analysis.
• English: excellent written and oral communication skills; fluency in one or more additional European languages.
• IT skills: Microsoft Office, ideally also CI fitting software, statistics software, and Matlab.

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