Clinical Content Automation Lead

Novo Nordisk A/S

Søborg

On-site

DKK 743,000 - 1,092,000

Full time

14 days+

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Job summary

Novo Nordisk A/S invites applications for a Document Automation Specialist in Søborg, Denmark. You will drive content digitalisation and automation initiatives across Clinical Reporting, shaping regulatory content creation while aligning with long-term strategy.

You will lead automation projects, develop content libraries, and partner with stakeholders to streamline documentation processes, ensuring high quality and scalable outputs for global regulatory needs.

Qualifications

  • Master's or PhD in a scientific field with industry relevance.
  • 5+ years as Medical Writer or equivalent in pharma.
  • Experience driving process improvements and automation projects.
  • Strong stakeholder management and cross-functional collaboration.
  • Ability to work independently and think strategically.
  • English fluency in writing and speaking.

Responsibilities

  • Lead document automation initiatives to enable scalable content reuse across regulatory and clinical documentation.
  • Develop and maintain content libraries; advance digital tools and automation solutions.
  • Collaborate with cross-functional stakeholders to optimise documentation processes and drive efficiency.
  • Serve as a domain expert in content automation aligned with Clinical Reporting strategy.
  • Guide organisational change, training, and multidisciplinary project leadership through complex transformations.

Skills

Content automation
Stakeholder mgmt
English fluency
Advanced degree
Strategic thinking
Independent work

Education

Master's or PhD in science

Tools

Content automation tools
Document mgmt systems

Job description

Novo Nordisk A/S invites applications for a Document Automation Specialist in Søborg, Denmark. You will drive content digitalisation and automation initiatives across Clinical Reporting, shaping regulatory content creation while aligning with long-term strategy.

You will lead automation projects, develop content libraries, and partner with stakeholders to streamline documentation processes, ensuring high quality and scalable outputs for global regulatory needs.

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