Clinical Evaluations Manager (m/f/d)

JR Germany; Mönchengladbach; Vor Ort; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

JR Germany is seeking a Clinical Evaluations Manager to join their team. This role involves assessing the safety and performance of medical devices and requires strong scientific writing skills and a Master’s degree in a relevant field. The position offers a dynamic international environment and flexible hours.

Leistungen

Central Location

Employee Discounts

Flexible Hours

International Environment

Onboarding

Workplace Well-Being

Qualifikationen

• Master’s degree or higher required.
• Demonstrable scientific writing experience.
• Experience with Regulatory Affairs is desirable.

Aufgaben

• Create, edit, and proofread clinical evaluations.
• Conduct literature reviews for regulatory submissions.
• Collate and analyze clinical data from multiple sources.

Kenntnisse

Scientific writing

Analytical skills

Communication skills

Ausbildung

Master’s degree in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences

Jobbeschreibung

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Client:

MED-EL

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Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

About MED-EL

MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,900 employees around the world.

Clinical Evaluations Manager (m/f/d)
Clinical Research
Innsbruck, Austria | Professionals | Full-Time 38.5h | Limited 30-Nov-2027

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
• Acquire in-depth knowledge of MED EL products
• Conduct literature reviews to identify clinical data relevant to regulatory submissions
• Collate and analyze clinical data from clinical trials, scientific literature, product testing, and post-market experience
• Collaborate 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
• Demonstrable scientific writing experience
• Experience with Regulatory Affairs is desirable
• Excellent verbal and written communication skills in English; German is a plus
• Demonstrated understanding of, and enthusiasm for, scientific work and clinical research

Your Benefits

• Central Location
• Employee Discounts
• Flexible Hours
• International Environment
• Onboarding
• Workplace Well-Being

Interested?

Want to join a company that helps bring the joy of sound to people with hearing loss? Apply now!

Please apply in English!

Your Contact Person
If you have any questions please contact Marina Engl.
[emailprotected]