We are currently looking for an experienced Regulatory, Scientific, and Medical Writer to join an award-winning. Responsibilities: • Preparing a range of documents for submissions in the UK, EU and US such as clinical summaries and overviews, scientific advice briefing documents, paediatric investigation/study plans, orphan drug applications • Preparing clinical documents • Preparing abstracts and manuscripts for submissions for scientific conferences and publication in scientific journals • Registering clients and preparing and uploading data updates, to ensure compliance with local regulations • Project management/liaising internally and externally, to ensure client timelines are met • Scheduling and chairing roundtable meetings with clients to address and resolve comments on draft documents • Support for formatting of all document types, as required Contact Stephanie Maccioni on 01438 768713 or email [email protected], quoting job ref 50036.