Novo Nordisk is looking for an experienced medical writer for a permanent, office-based role in Clinical Reporting in Søborg.
The role
- Plan, develop and oversee regulatory and clinical documents such as study protocols, informed consent forms, investigator’s brochures, clinical summaries and paediatric plans.
- Develop briefing packages and responses to health authority questions.
- Represent Clinical Reporting in cross-functional project teams on document planning, requirements and data presentation.
- Work with Medical & Science, Regulatory Affairs, Clinical Operations, Biostatistics and Pharmacovigilance.
Requirements
- Master’s degree in natural sciences (MSc, MSc Pharm or equivalent), preferably with a PhD and/or pharmaceutical industry experience.
- A track record of driving complex tasks from start to end across many stakeholders.
- Strong scientific communication, and a good understanding of clinical development, regulatory processes and clinical documents.
- Full proficiency in spoken and written English. The ad is in English and states no Danish requirement.
About the employer
Clinical Reporting is Novo Nordisk’s medical writing function, with more than 200 medical writers worldwide, within Novo Development, which manages clinical drug development and submissions to health authorities. Permanent position, office-based in Søborg, working with colleagues in Denmark and abroad.
Salary and deadline
Annual base salary 651,000 to 956,900 DKK, depending on the level of the position. Application deadline: 15 November 2026; applications are reviewed on an ongoing basis. No cover letter needed; add a few sentences on motivation in the CV and leave out a photo.
Source: Novo Nordisk, “Experienced Medical Writer, Regulatory, Quality & Clinical Reporting, Søborg, Denmark”, read on 25 October 2026. Summary by AVIDE; see the original page for the full, current text.