Regulatory Content Writer: Pharma Automation & Compliance

Novo Nordisk A/S; Søborg; Remote; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk A/S is seeking a Regulatory Content Writer to transform regulatory documents using NovoScribe and structured authoring. You will drive document processes and deliver high-quality content through automation and governance.

You will collaborate with Clinical Reporting and Development teams across geographies to plan timelines, ensure scientific rigor, and maintain a growing regulatory text library. The role emphasizes continuous learning and career development opportunities.

Qualifications

• MSc degree in Life Sciences or related field.
• Excellent written English with ability to communicate complex scientific information clearly.
• Ability to improve processes and promote sharing of better practices.
• Strong stakeholder management, collaboration and project coordination skills.
• Strong analytical capabilities with attention to detail.
• Interest in challenging established ways and driving continuous improvement.

Responsibilities

• Drive development of regulatory documents in line with 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 understanding of regulatory, scientific, and medical subjects related to drug development.

Skills

Excellent English

Stakeholder management

Collaboration

Project coordination

Analytical skills

Attention to detail

Continuous improvement

Education

MSc degree in Life Sciences or related

Job description

Novo Nordisk A/S is seeking a Regulatory Content Writer to transform regulatory documents using NovoScribe and structured authoring. You will drive document processes and deliver high-quality content through automation and governance.

You will collaborate with Clinical Reporting and Development teams across geographies to plan timelines, ensure scientific rigor, and maintain a growing regulatory text library. The role emphasizes continuous learning and career development opportunities.