Regulatory Content Writer: Drive Automated Pharma Documentation

Cari; Søborg; Remote; DKK 570,000 - 838,000; Full time

Job summary

Cari in Søborg, Denmark, invites applications for a Regulatory Content Writer to advance regulatory documents using NovoScribe, Novo’s automated authoring platform. You will drive document processes and deliver high-quality regulatory content through automation and structured authoring.

The role requires an MSc in Life Sciences or related field, excellent written English, and strong skills in stakeholder management, coordination, and analytical thinking.

Qualifications

• MSc degree in Life Sciences or related field.
• Excellent written English.
• Ability to improve processes and promote best practices.
• Strong stakeholder management and project coordination skills.
• Strong analytical capabilities and attention to detail.
• Proactive mindset and passion for continuous improvement.

Responsibilities

• Drive development of regulatory documents per guidelines and SOPs.
• Plan content creation and set timelines for production and review.
• Evaluate documents for coherence, precision, and scientific rigour.
• Maintain and expand the text library in the database.
• Improve best practices and innovate the way we work.
• Stay updated on regulatory, scientific, and medical topics relevant to drug development.

Skills

Excellent written English

Stakeholder management

Project coordination

Analytical capabilities

Process improvement

Education

MSc degree in Life Sciences or related field

Job description

Cari in Søborg, Denmark, invites applications for a Regulatory Content Writer to advance regulatory documents using NovoScribe, Novo’s automated authoring platform. You will drive document processes and deliver high-quality regulatory content through automation and structured authoring.

The role requires an MSc in Life Sciences or related field, excellent written English, and strong skills in stakeholder management, coordination, and analytical thinking.