Medical Writer

1 month ago


London, Greater London, United Kingdom Publicisgroupe Full time

At Publicis Groupe, we are seeking a highly skilled Medical Writer to join our team for a 3-month period. As a native Swedish speaker, you will be responsible for translating complex scientific and clinical information into clear and concise documents for our clients in the pharmaceutical industry.

The ideal candidate will have a strong background in medical writing, with a minimum of 10 years of experience in the field. A PhD is preferred, but not required. Your primary responsibility will be to communicate medical and scientific information to various audiences, including healthcare professionals, regulatory agencies, and the public.

Key responsibilities will include:

  • Preparing and editing clinical study protocols, clinical study reports, investigator brochures, and other regulatory documents for submission to health authorities.
  • Ensuring that these documents comply with regulatory guidelines and standards.
  • Contributing to the development of manuscripts, abstracts, and posters for publication in scientific journals and presentations at conferences.
  • Communicating complex scientific and medical information in a clear and understandable manner for diverse audiences.
  • Preparing safety-related documents such as periodic safety update reports (PSURs), risk management plans, and other safety documents required for regulatory submissions.
  • Collaborating with cross-functional teams to compile and write sections of regulatory submissions, such as New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), and Investigational New Drug (IND) applications.

We offer a dynamic and supportive work environment, with opportunities for professional growth and development. If you are a highly motivated and experienced medical writer looking for a new challenge, we encourage you to apply for this exciting opportunity.



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