Job Description

Department: MRQ

Location: Beijing

The position

• Perform medical writing tasks for regulatory documents (e.g., HA consultation package, bridging report, clinical summaries), including Chinese version proofreading.
• Take overall responsibility to drive local clinical trial disclosure on specific trial/project.
• Contribute to knowledge sharing, skill building and good collaboration with stakeholders and colleagues.

Qualifications

• Master degree or above in clinical medicine or health-related science.

• Experience with scientific research methodology, including designing and conducting experiments, and analysing and reporting experimental results.
• ≥2 years of experience with a broad range of scientific writing tasks; experience from the pharmaceutical industry is a major advantage but not a must.
• Experience of project management is an asset.

• Ability and flexibility to plan and prioritise on complex tasks, multiple tasks and changing deadlines; to approach it business oriented.
• Ability to work effectively as a team player as well as independently.
• Excellent communication skills.

• Fluent English in both written & verbal.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.