Regulatory Content Writer: Automation & Standards

Novo Nordisk; Gladsaxe Kommune; On-site; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk in Søborg, Denmark, seeks a Regulatory Content Writer to transform regulatory documents using NovoScribe and automated authoring. You will drive document processes and deliver high-quality content through automation and structured authoring, shaping how complex scientific information is communicated across clinical development.

You will collaborate with multi-disciplinary teams, maintain regulatory knowledge, and contribute to continuous improvement initiatives that create

Qualifications

• MSc degree in Life Sciences, Pharmacy, Biology, Biochemistry, Medicine or a related scientific discipline.
• Excellent written English, with ability to communicate complex scientific information clearly.
• The ability to improve processes and promote sharing of better practices.
• Strong stakeholder management, collaboration and project coordination skills.
• Strong analytical capabilities, attention to detail, intellectual curiosity and a proactive mindset.
• Enjoyment in challenging established ways of working and contributing to continuous improvement initiatives.

Responsibilities

• Drive the development of regulatory documents in line with established guidelines and SOPs.
• Plan content creation and set timelines for document production and review.
• Evaluate documents for coherence, precision, scientific rigour, and consistent information and messaging.
• Maintain and expand the text library in the database, and provide input to improve the database.
• Actively improve best practices and innovate the way we work.
• Maintain an updated understanding of essential regulatory, scientific, and medical subjects pertinent to drug development.

Job description

Novo Nordisk in Søborg, Denmark, seeks a Regulatory Content Writer to transform regulatory documents using NovoScribe and automated authoring. You will drive document processes and deliver high-quality content through automation and structured authoring, shaping how complex scientific information is communicated across clinical development.

You will collaborate with multi-disciplinary teams, maintain regulatory knowledge, and contribute to continuous improvement initiatives that create