Medical Writer

Job summary

This role involves transforming evidence from clinical studies and related activities into clear regulatory documentation and publications to support market access and adoption for healthcare products. The position is based in Humlebæk, Denmark, within a dedicated Medical Writing & Biostatistics team.

Qualifications

• University degree in healthcare, medical, or life sciences; PhD preferred.
• Exceptional written English communication skills, with clarity and conciseness.
• Experience in medical writing, ideally in the pharma/medtech industry, focusing on clinical study reporting and publication in peer-reviewed journals.

Responsibilities

• Author and submit manuscripts and abstracts to biomedical journals and conferences.
• Conduct literature reviews and contribute to study design.
• Produce compliant clinical documentation for regulatory purposes.
• Collaborate with internal and external stakeholders to shape scientific publications.
• Develop and improve internal processes and best practices within the team.

Skills

• Strong attention to detail and structured task management.
• Ability to convey complex information clearly and concisely.
• Proactive and solution-oriented approach to work.
• Comfortable engaging with diverse stakeholders to facilitate decision-making.

Education

• University degree in health care, medical, or life sciences; PhD preferred.

Tools

• Familiarity with clinical documentation and publication processes.