Medical Writer (Maternity cover)

Opportunity summary

Regulatory, Quality & Clinical Reporting Søborg, Denmark Are you passionate about combining your scientific expertise with impactful communication through high-quality clinical documentation that supports the development of innovative healthcare solutions? Do you thrive in a collaborative and global environment where scientific expertise, strategic mindset, stakeholder management, and communication skills go hand in hand? If so, this may be the opportunity for you. Your New Role This is a one-year temporary position in Clinical Reporting, Medical Writing, Diabetes and Obesity. In this role, your main responsibility will be to drive the preparation of complex clinical documents and act as a project manager. More specifically, you will: Plan, develop, and oversee regulatory documents, including study protocols, informed consent forms, investigator’s brochures, clinical summaries, pediatric plans, briefing packages, and responses to health authority questions according to business needs. Represent Clinical Reporting in cross-functional project teams and provide guidance on planning regulatory documents, document requirements, and optimal data presentation. Collabor1 …

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