Your role As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development Execution Services department responsible for medical writing aspects of our clinical development projects including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities.
You write and coordinate the development of briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, pediatric investigational plans, clinical overviews and summaries, safety...