Medical Writer (Novo Nordisk)
6/4/20261 min read
Roles and Responsibilities
Key responsibilities
Efficiently manage and deliver on clinical reporting and medical writing deliverables while maintaining high quality standards.
Implement project strategies into documents and review project/study-specific materials as needed.
Engage stakeholders to identify needs, timing and scope of clinical reporting deliverables and ensure alignment with the Clinical Reporting strategy.Support execution of the Clinical Reporting vision and contribute to process improvements and efficiency initiatives.
Share knowledge, mentor colleagues, and contribute to training activities to build capability across the team.
Apply a quality mindset and maintain up-to-date knowledge of global regulatory requirements and policies relevant to your work.
Your Skills and Qualifications
To be successful in this role, you should have the following qualifications:
Must have PhD, Medical degree or Master’s degree (MSc, M Pharm, Pharm D or equivalent) combined with relevant experience.
Experience: At least 2 years’ experience in regulatory medical writing
Experience across a broad range of scientific writing tasks; experience in the pharmaceutical industry or equivalent is desirable
Able to work independently on well-defined tasks with appropriate guidance, strong analytical skills, persistence, accountability, and ability to manage variable workloads.
Communication: Fluent in written and spoken English with the ability to translate complex scientific data into clear, concise, and engaging content tailored to diverse audiences.
Collaboration & stakeholder management: Good project management skills; skilled at fostering cross-functional collaboration across multidisciplinary teams and maintaining professional, trustworthy communication with integrity.
Additional attributes: Cultural awareness for global collaboration, willingness to seek feedback and continuously improve, and a quality-focused mindset.
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