MED-EL

Clinical Evaluations Manager (m/f)

CRD_1_1812

Innsbruck, Austria

Main Tasks

  • Create, edit, and proofread Clinical Evaluation Reports 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

 

Requirements

  • University degree in Life Sciences, 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

 


Salary will be determined based on professional experience; the formal minimum salary according to Collective Bargaining Agreement is EUR 36,154.72


We offer a challenging opportunity in a multinational work environment with English as our company language. We look forward to receiving your application at jobs.medel.com

 


 

 

 

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