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For a company in the medical device industry, we are looking for an experienced Freelance Medical Writer / Clinical Evaluation Specialist (m/f/d) to provide long-term, project-based support in clinical documentation.
Responsibilities
Support the preparation and updating of Clinical Evaluation Reports (CER/CEV)
Conduct structured literature searches
Review and critically evaluate relevant scientific and clinical literature
Support the preparation and documentation of clinical data for regulatory and technical documentation
Contribute to recurring and annual clinical documentation activities
Collaborate with internal stakeholders from Clinical, Regulatory and Medical functions
Clinical Focus
The products are therapeutic medical devices used primarily in areas such as:
Urology, including the treatment of stone diseases and tissue-related indications
Orthopaedic applications
Specific product or device knowledge is not mandatory. Appropriate product onboarding will be provided.
Requirements
Several years of experience in Medical Writing and/or Clinical Evaluation of Medical Devices
Strong experience in literature research and literature evaluation
Experience in preparing or contributing to Clinical Evaluation Reports (CER/CEV)
Good understanding of clinical documentation within the medical device environment
Medical or scientific background
A degree in Human Medicine / medical qualification is strongly preferred
Independent and structured working style
Flexibility to support the project on an on-demand basis
Project Details
Start: January 2027
Workload: approx. 10–15 hours per month on average
Location: Remote
Duration: Long-term collaboration intended
Workload model: Flexible, on-demand support with varying workload
Periods of increased short-term workload may be followed by several weeks without project activity
Recurring annual reporting activities will form part of the assignment
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