Clinical Evaluations Manager (m/f/d)

JR Germany; Bielefeld; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

A leading medical device company is seeking a Clinical Evaluations Manager to enhance the assessment of its innovative products. Ideal candidates will possess a Master's degree in relevant sciences and experience in scientific writing. This full-time position offers a supportive international work environment and various employee benefits.

Leistungen

Central Location

Employee Discounts

Flexible Hours

International Environment

Onboarding Program

Workplace Well-Being

Qualifikationen

• Master’s or higher degree in relevant scientific field required.
• Experience in scientific writing necessary.
• Regulatory Affairs experience is a plus.

Aufgaben

• Create and proofread clinical evaluations for MED-EL products.
• Conduct literature reviews for regulatory submissions.
• Analyze clinical data from various sources.

Kenntnisse

Scientific writing

Communication in English

Interest in scientific research

Ausbildung

Master’s or higher in Life/Natural Sciences

Master’s or higher in Healthcare

Master’s or higher in Medicine

Master’s or higher in Engineering

Master’s or higher in Technical Sciences

Jobbeschreibung

Social network you want to login/join with:

Clinical Evaluations Manager (m/f/d), Bielefeld

Client: MED-EL

Location: Bielefeld, Germany

Job Category: Other

EU work permit required: Yes

Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

About MED-EL

MED-EL is a leading manufacturer of innovative medical devices for treating hearing loss. Our portfolio of implantable hearing solutions benefits thousands worldwide. Headquartered in Innsbruck, Austria, MED-EL employs over 2,900 people globally.

Clinical Evaluations Manager (m/f/d)

Location: Innsbruck, Austria | Full-Time | 38.5 hours/week | Limited until 30-Nov-2027

Your Tasks

• Create, edit, and proofread clinical evaluations to assess the safety and performance of MED-EL products, complying with regulations.
• Gain in-depth knowledge of MED-EL products.
• Conduct literature reviews to identify relevant clinical data for regulatory submissions.
• Analyze clinical data from trials, literature, product testing, and post-market data.
• Collaborate with internal departments and external partners.

Your Profile

• Master’s or higher degree in Life/Natural Sciences, Healthcare, Medicine, Engineering, or Technical Sciences.
• Experience in scientific writing.
• Regulatory Affairs experience is a plus.
• Excellent English communication skills; German is a bonus.
• Strong interest in scientific research and clinical work.

Your Benefits

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

Interested?

Join a company dedicated to improving hearing health. Apply now! Please submit your application in English.

Your Contact Person

For questions, contact Marina Engl at [emailprotected].