Senior Medical Writer — Regulatory Submissions Lead
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IQVIA is seeking a Principal Medical Writer to lead the development of regulatory documents for global submissions. You will guide cross-functional teams, ensuring scientifically rigorous, data-accurate, and well-presented documents such as IBs, CSRs, and submission dossiers.
You will oversee the writing of summary documents, manage timelines, and contribute to process improvements across multiple compounds. A strong background in clinical development and regulatory standards is essential.