About this role

Planning and execution of clinical trials for Oticon Medical hearing solutions
Drive submissions and correspondence with ethical committee and competent authorities
Complete documentation for clinical trials according to regulations
Secure high data quality by relevant monitoring activities
Build and maintain a study database
Analyze, summarize, and disseminate clinical trial data
Contribute to further improvements in internal procedures for clinical trials
Act as a subject matter expert in audiology and support colleagues with study design decisions, choice of hearing outcomes, and clinical know-how.
Expect 15-30 days of business travel per year with variation depending on project and phase.

Trained Audiologist
University degree in Audiology, Medicine, Life Science, or similar field
Operational experience from working with clinical trials of medical devices
Specific know-how around study design, execution, and result dissemination from both pre
and post-market clinical trials
Good understanding of relevant steering regulations (e.g., ISO14155, Good Clinical Practice)
Fluent in English
Strong communication skills
Ability to build strong relationships and collaborate with researchers and healthcare professionals
Pragmatic and commercial mindset
Result-oriented and attention to detail and the bigger picture

Clinical Trial Manager – Audiology

Key skills