Medical Writer jobs in Germany

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The Senior Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas.

• Plan and deliver regulatory submissions on behalf of pharmaceutical clients
• Prepare clinical regulatory documents across multiple therapy areas
• Evaluate scientific data
• Work on projects independently as well as group projects

You

To apply for this role as Senior Regulatory Writer our client is hoping for someone with the following skills and experience

• Ample regulatory writing experience within a pharmaceutical company, CRO or Consultancy
• Experience writing clinical regulatory documents to a high standard
• Strong understanding of clinical development and ICH guidelines
• Experience authoring regulatory documentation such as CTD modules, response documents and regulatory briefing documents
• Degree educated in life sciences / pharmaceutical science