Medical Writer

☞ Real Staffing

見る: 165

更新日: 26-11-2025

場所: Liège City Liège

カテゴリー: 印刷

業界: Medical Devices

レベル: Entry level

ジョブタイプ: Full-time

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仕事内容



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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締切: 10-01-2026

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