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Medical Writer
View: 165
Update day: 26-11-2025
Location: Liège City Liège
Category: Printing / Publishing
Industry: Medical Devices
Position: Entry level
Job type: Full-time
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Job content
Responsibilities
- Preparing, writing, editing, and reviewing regulatory (e.g. Clinical Evaluation Reports (CERs), clinical data reports or summaries) documents.
- PMS data analysis and preparation of PMS reports for submission to EUDAMED
- Strong medical and technical writing skills ie. Investigational brochures preparation, clinical study reports drafts
- Knowledge and understanding of proposed and current global regulations and guidance and the ability to relay the impact of such regulations and guidance internally.
- Ensures documents are produced in accordance with procedures, internal and external guidelines (e.g. MDR)
- Knowledge of clinical research and regulatory requirements
- Literature reviews of specific medical devices (preferably in ophtalmology)
- Preparation of scientific publications, abstracts and conference presentations
- Writing of congresses reports
Requirements
- 3+ years of experience within the medical device industry: CRO, investigational center, ophthalmic device (preferably IOL) manufacturer
- Knowledge of clinical evaluation report regulatory requirements, evidence generation, and CER document creation
- Or 3 - 5 year’s industry experience in medical writing in the healthcare industry or academia or in a related area such as quality, regulatory or clinical research
- Experience with international regulation agencies, requirements and guidance associated with clinical regulatory document preparations, submissions and reporting is preferred.
- Fluency in English is a must
- Knowledge of any of the following language is an asset: German, French, Japanese
Behaviors
Action-Oriented, Approachability, Building Effective Teams, Composure, Customer Focus, Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning
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Deadline: 10-01-2026
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