Regulatory Affairs
Regulatory Content Writer
Summary
The Regulatory Content Writer develops and evaluates regulatory documents, maintains a text library, and improves automated authoring processes and digital tools for clinical development.
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Opportunity summary
Pay: 570,200–838,100 DKK per year. Country: Denmark.
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 You enjoy combining scientific expertise with innovation, technology and collaboration.
- You thrive in a dynamic environment, take ownership of your work and are motivated by improving how complex scientific information is communicated.
To succeed in this role, you will 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 practices1 …
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