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Gladsaxe, Gladsaxe Municipality, Denmark Novo Nordisk AS Full time

At Novo Nordisk A/S, we are committed to delivering innovative solutions for patients worldwide. As a Medical Writing Specialist, you will be part of our Clinical Reporting team, responsible for creating high-quality clinical documents that meet the highest standards of regulatory compliance.

The position involves planning and preparing complex clinical documents, including study protocols, informed consent forms, investigator's brochures, and clinical summaries. You will work closely with cross-functional teams to ensure that all source information and data are accurately reported in terms of accuracy, completeness, and scientific interpretation.

To succeed in this role, you must have a Master's degree within natural sciences (M.Sc., M.Sc. Pharm. or equivalent), supplemented with a PhD (preferably) and at least 3 years of relevant experience in the pharmaceutical industry. You should also demonstrate expertise in communicating scientific information, tailoring it to meet diverse objectives, and improving processes.

We offer a dynamic work environment where collaboration and innovation are encouraged. Our supportive culture drives business transformation, and we value continuous learning, being bold, and striving for simplicity.

Clinical Reporting covers all clinical drug development projects across therapy areas. Our main focus is to use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials, and our main task is to ensure communication of clinical data in a clear and concise manner.