Medical Writing Specialist shaping scientific communication across global clinical development. Delivering high-quality clinical documentation and influencing strategic decisions in the pharmaceutical industry.
Responsibilities
Deliver a broad range of regulatory medical writing tasks to a consistently high standard
Act as Clinical Reporting Project Lead or Medical Writing Lead on assigned projects, ensuring alignment across stakeholders
Represent Medical Writing in cross-functional discussions and project groups
Share better practices, mentor colleagues, and contribute to capability building
Lead process optimisation initiatives and help develop innovative solutions that support our strategic ambitions
Requirements
Master’s degree within natural sciences (e.g., M.Sc., M.Sc. Pharm., or equivalent) ideally supplemented with a PhD
At least 5 years of relevant medical writing experience in the pharmaceutical industry
Expert understanding of clinical development, regulatory requirements, and clinical documentation
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