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Clinical Evaluations Manager
vor 4 Wochen
Your Tasks- Create, edit, and proofread Clinical Evaluations 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
- Conduct literature reviews to identify clinical data relevant to regulatory submissions
- Collate and analyse clinical data from clinical trials and testing, scientific literature, and post-market experience
- Liaise with other departments within MED-EL, and with external partners
- Your Profile- Masters’ degree or higher degree (University, FH) in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences
- Demonstrable scientific writing experience
- Experience with Regulatory Affairs desirable
- Excellent verbal and written communication skills in English, and preferably also in German
- Demonstrated understanding of, and enthusiasm for, scientific working and clinical research
Your Benefits
- Central Location- Employee Discounts- Flexible Hours- International Environment- Onboarding- Workplace Well-Being- Further information
- Minimum SalaryAnnual gross salary from € 50,018.16, based on professional qualification and experience.
- Earliest Entry DateThis position is to be filled immediately.
- Temporary PositionThis position is limited until 31-May-2024.
- Your Contact PersonIf you have any questions please contact Marina Engl.
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