OverviewAs a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape scientific communication and contribute to improving patient outcomes on a global scale.Retribuzione / Benefitscompetitive salary package (GBP)flexible options depending on experienceon-site rolecollaborative environmentResponsabilitàLead development and review of clinical and regulatory documents ensuring compliance with industry standardsManage multiple projects with timelines and deliverables across teamsBuild strong working relationships with clinical and regulatory personnel to streamline information flowDrive innovative approaches to scientific writing for clarity and impactAnalyze and interpret complex data to produce concise documentationMaintain up-to-date knowledge of regulatory requirements and industry best practicesRequisiti fondamentaliExtensive experience in medical or scientific writing within the life sciencesProven ability to manage large, complex documentation projectsExcellent understanding of regulatory guidelines and submission processesStrong communication skills and attention to detailProficiency with relevant document management tools and softwareRelevant certifications or advanced degrees in life sciences are preferredStrong communicationAttention to detailCross-functional collaborationDocument management tools and software

📌 Principal/Head Of Medical Writing (Ponderano)
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📍 Ponderano