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Manager of Scientific Medical Writing

My leading Biotech client

Apply before: May 8, 2024
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  • Date posted
    March 9, 2024
  • Location
    Onsite
  • Apply before
    May 8, 2024
  • Career Level
    Manager

Job Description

Description

My leading Biotech client is seeking a highly skilled Manager of Scientific Medical Writing to join their team in Mainz, Germany. In this critical position, you will provide hands-on expertise to deliver high-quality clinical documents that effectively communicate science and meet regulatory requirements.

Responsibilities:

  • Work in a team of medical writers writing clinical study protocols, clinical study reports, investigator brochures, and more
  • Provide hands-on medical/scientific writing and authoring for regulatory submissions and publications
  • Coach and mentor medical writing staff and ensure quality standards are consistently met
  • Partner cross-functionally with clinical operations, regulatory affairs, statistics, and medical teams
  • Develop SOPs, and style guides, and optimize processes for medical writing activities
  • Establish timelines, provide status updates, and ensure on-time delivery of writing projects

Requirements

Requirements:

  • PhD in life sciences or related field with 5+ years of medical writing experience in the biopharma industry
  • Expert knowledge of ICH guidelines and experience with global regulatory submissions
  • Leadership skills with a hands-on approach to managing multiple projects and priorities
  • Excellent time management, communication, collaboration, and problem-solving skills
  • Proficiency in MS Office; experience with document management systems
  • Fluent in English and German (written and verbal)

Benefits

  • Private Health Insurance
  • Pension Plan
  • Paid Time Off
  • Training & Development
  • Performance Bonus