RDCE_12605
Innsbruck, Austria
Professionals
Full-Time 38.5 h
Tasks
* Oversee the planning, execution, and maintenance of clinical evaluation activities to ensure compliance with regulatory requirements and company standards
* Collate and analyze clinical data from clinical trials and testing, scientific literature, and post-market experience
* Create, edit, and proofread Clinical Evaluation Reports and associated documents to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations
* Build up the necessary knowledge regarding MED-EL products
* Collaboration with other departments within MED EL, and with external partners
Profile
* Master’s degree or higher degree (University, FH) in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences
* Proven experience in scientific writing
* Experience in regulatory affairs is beneficial
* Excellent communication skills in English both written and spoken; German skills are desirable
* Understanding of, and enthusiasm for scientific working, medical technology, and clinical research
Benefits
* Central Location
* Employee Discounts
* Flexible Hours
* Home Office
* International Environment
* Onboarding
Further Information
Minimum Salary: Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is € 47,810.14.
Earliest Entry Date: This position is to be filled by 03. Aug. 2026.
Your Contact Person: If you have any questions, please contact Marina Engl.
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