Senior Medical Writer

il y a 4 semaines


France Barrington James Temps plein

A fast-growing global AI company is seeking an experienced Medical Writer with a background in pharmacovigilance to join their innovative team. This hands-on role focuses on leveraging AI and automation to streamline regulatory document creation while maintaining the highest quality standards.Key Responsibilities:Develop and maintain templates and content models for automated regulatory documentsReview and validate AI-generated safety reports for accuracy and complianceCollaborate with product, engineering, and regulatory teams to improve workflowsEnsure outputs meet global regulatory standards (FDA, EMA, ICH, and others)Keep up-to-date with industry trends and regulatory updates to support automation improvementsRequirements:5+ years of experience in medical writing, with a focus on pharmacovigilance documentsStrong knowledge of PV regulations, clinical documents, and safety databasesExperience with structured data, document automation, or AI-driven content is a plusExcellent attention to detail, communication, and collaboration skillsAbility to manage multiple projects and meet deadlines in a fast-paced environmentThis is a unique opportunity to combine medical writing expertise with cutting-edge AI technology, helping transform regulatory document workflows globally.If you’re interested in learning more, feel free to reach out or apply below:✉ lcattcamfield@barringtonjames.com☎ +44 (0) 1293 776644


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