Medical Writer
Novo Nordisk
full-time
Posted on:
Location Type: Office
Location: Beijing • China
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About the role
- 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.
Requirements
- 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.
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical writingregulatory documentsscientific research methodologyexperimental designdata analysisscientific reportingclinical trial disclosureproject managementproofreadingclinical summaries
Soft Skills
collaborationknowledge sharingskill buildingplanningprioritizationflexibilitybusiness orientationteam playerindependencecommunication
Certifications
Master degreeclinical medicinehealth-related science