Denmark Job Openings

Novo Nordisk
Medical Writer (Maternity Cover)
Søborg
November 22, 2024
- Planning, development, and oversight of regulatory documents, including study protocols, informed consent forms, investigator’s brochures, clinical summaries, paediatric plans, briefing packages, and responses to health agency questions according to business needs.
- Representing Clinical Reporting on cross-functional project teams and providing guidance on regulatory document requirements and optimal data presentation.
- Working collaboratively with other job functions across Development (notably Biostatistics, Pharmacovigilance, Medical & Science, Regulatory Affairs, Clinical Operations, and others), ensuring all source information and data are appropriately reported in terms of accuracy, completeness, and scientific interpretation - all in accordance with project timelines.
- A master’s degree within natural sciences (MSc., MSc. Pharm. or equivalent), preferably supplemented with a Ph D and/or relevant experience in the pharmaceutical industry.
- A track record of driving your own complex tasks from start to end, navigating many different stakeholders, and are an expert in communicating scientific information.
- The ability to improve processes and to promote the sharing of better practices.
- An expert understanding of clinical development, regulatory processes & requirements, and clinical documents.
- Full proficiency in spoken and written English.
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