Senior Medical Writer

il y a 20 heures


Paris, 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 documents Review and validate AI‑generated safety reports for accuracy and compliance Collaborate with product, engineering, and regulatory teams to improve workflows Requirements 5+ years of experience in medical writing, with a focus on pharmacovigilance documents Strong knowledge of PV regulations, clinical documents, and safety databases Experience with structured data, document automation, or AI‑driven content is a plus Excellent attention to detail, communication, and collaboration skills Ability to manage multiple projects and meet deadlines in a fast‑paced environment This 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: Seniority level Mid‑Senior level Employment type Full‑time Job function Writing/Editing Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr


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