Regulatory Content Writer

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

Benefits offered by this job

Incentives and benefits

Career development opportunities

Job summary

Novo Nordisk is seeking a Regulatory Content Writer in Søborg, Denmark. You will drive automated authoring for regulatory documents using NovoScribe, plan content timelines, and ensure coherence, precision, and scientific rigour across documents. You will maintain the text library and push process improvements while staying updated on regulatory topics.

The role emphasizes collaboration with cross-functional teams and continuous development within a global healthcare company.

Qualifications

• MSc in Life Sciences, Pharmacy, Biology, Biochemistry, Medicine or related field.
• Excellent written English with ability to convey complex scientific information clearly.
• Ability to improve processes and promote better practices.
• Strong stakeholder management, collaboration and project coordination skills.
• Analytical, detail-oriented, curious and proactive.
• Willingness to challenge established ways and contribute to continuous improvement.

Responsibilities

• Drive development of regulatory documents following guidelines and SOPs.
• Plan content creation and set timelines for production and review.
• Evaluate documents for coherence, precision, scientific rigour and messaging.
• Maintain and expand the text library and contribute to database improvements.
• Improve best practices and innovate working methods.
• Keep updated on regulatory, scientific and medical topics relevant to drug development.

Education

MSc degree in Life Sciences or related scientific discipline

Excellent written English

Process improvement mindset

Stakeholder management & coordination

Analytical rigor and attention to detail

Proactive mindset and adaptability

Tools

NovoScribe

Job description

Job Title: Regulatory Content Writer

Department: Content Innovation & Management, Clinical Reporting, Research & Development

Location: Søborg, Denmark

Your impact begins here

As Regulatory Content Writer, you will play a key role in transforming the way regulatory documents are created in the pharmaceutical industry. Working with NovoScribe, Novo's automated authoring platform, you will drive document processes and deliver high-quality regulatory content through automation and structured authoring. Your work will help accelerate the adoption of content automation, strengthen content quality and shape how complex scientific information is communicated across clinical development.

What you'll bring

• An MSc degree in Life Sciences, Pharmacy, Biology, Biochemistry, Medicine or a related scientific discipline.
• Excellent written English, with a demonstrated ability to communicate complex scientific information clearly and accurately.
• The ability to improve processes and promote the sharing of better practices.
• Strong stakeholder management, collaboration and project coordination skills, with the ability to manage multiple priorities effectively.
• 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 that create meaningful business impact.

What you'll do

• 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, designated products, and specific disease/therapeutic domains.

Who you'll work with

You will join Content Innovation & Management within Clinical Reporting, a globally connected organisation that advances how scientific and regulatory content is created, managed, standardised and delivered. The team works across multiple functions and geographies to drive innovation, strengthen content quality and support the clinical development value chain through modern digital tools and ways of working.

In Research & Development, colleagues explore bold scientific ideas and advance them into clinical testing, combining curiosity, AI tools and human data. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs. In this role, you will collaborate with cross-functional stakeholders to continuously improve processes, content libraries and digital tools.

What you can expect here

You will join a global healthcare company where you can contribute your expertise, build new skills and help shape the future approach to documentation across the organisation. We offer continuous learning, career development and benefits tailored to your life and career stage.

Salary

For this role, the Annual Base Salary ranges from 570,200.00 to 838,100.00 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate's skills, competencies, knowledge, and relevant experience.

Incentives and Benefits

• The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area, and relevant market benchmarks.

Learn more about our Reward Philosophy here.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.