Medical Writer
2 months ago
We are seeking a highly skilled Medical Writer to join our team at Publicis Denmark A/S. As a Medical Writer, you will be responsible for translating complex scientific and clinical information into clear and concise documents for our clients in the pharmaceutical industry.
Key Responsibilities:- Clinical and Regulatory Writing: Prepare and edit clinical study protocols, clinical study reports, investigator brochures, and other regulatory documents for submission to health authorities.
- Publication Writing: Contribute to the development of manuscripts, abstracts, and posters for publication in scientific journals and presentations at conferences.
- Scientific Communication: Communicate complex scientific and medical information in a clear and understandable manner for diverse audiences, including healthcare professionals, patients, and the general public.
- Drug Safety Documents: Prepare safety-related documents such as periodic safety update reports (PSURs), risk management plans, and other safety documents required for regulatory submissions.
- Regulatory Submissions: Collaborate 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.
- 10+ years of medical writing experience.
- PHD is preferred.
- Danish native speaker - Mandatory.
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