Clinical Evaluation Manager (m/f/d)
Your 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
Your 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
Further information about MED-EL can be found here .
Benefits
* Central Location
* Employee Discounts
* Flexible Hours
* Home Office
* International Environment
* Onboarding