Regulatory Medical Writing Lead – Clinical Documentation

Novo Nordisk A/S; Søborg; Remote; DKK 743,000 - 1,092,000; Full time

Job summary

Novo Nordisk A/S in Søborg, Denmark, is seeking an experienced Medical Writing Specialist to shape scientific communication across global clinical development. You will deliver high-quality regulatory documents and lead projects within Clinical Reporting, collaborating with global colleagues across functions and therapeutic areas.

The role requires a Master’s in natural sciences, 5+ years of medical writing in pharma, deep regulatory knowledge, and excellent English.

Qualifications

• Master’s degree in natural sciences or equivalent (MSc/MSc Pharm)
• Minimum 5 years of medical writing experience in pharma
• Strong understanding of clinical development and regulatory documentation
• Proficiency in written and spoken English

Responsibilities

• Deliver regulatory medical writing tasks to high quality standards
• Act as Clinical Reporting Lead on assigned projects and ensure stakeholder alignment
• Represent Medical Writing in cross-functional discussions and projects
• Mentor colleagues and contribute to capability building
• Lead process improvements and develop innovative solutions for strategic goals

Skills

Master? s degree in natural sciences

5+ years medical writing

Regulatory knowledge

English proficiency

Education

Master's degree in natural sciences

Job description

Novo Nordisk A/S in Søborg, Denmark, is seeking an experienced Medical Writing Specialist to shape scientific communication across global clinical development. You will deliver high-quality regulatory documents and lead projects within Clinical Reporting, collaborating with global colleagues across functions and therapeutic areas.

The role requires a Master’s in natural sciences, 5+ years of medical writing in pharma, deep regulatory knowledge, and excellent English.