14 ott - Perugia
Meet Life Sciences
pAs 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. /pullicompetitive salary package (GBP) /lilion-site role /liliLead development and review of clinical and regulatory documents ensuring compliance with industry standards /liliManage multiple projects with timelines and deliverables across teams /liliBuild strong working relationships with clinical and regulatory personnel to streamline information flow /liliDrive innovative approaches to scientific writing for clarity and impact /liliAnalyze and interpret complex data to produce concise documentation /liliMaintain up-to-date knowledge of regulatory requirements and industry best practices /liliExtensive experience in medical or scientific writing within the life sciences /liliProven ability to manage large, complex documentation projects /liliExcellent understanding of regulatory guidelines and submission processes /liliStrong communication skills and attention to detail /liliProficiency with relevant document management tools and software /liliRelevant certifications or advanced degrees in life sciences are preferred /liliStrong communication /liliCross-functional collaboration /liliDocument management tools and software /li /ulpPrincipal/Head of Medical Writing perugia, umbria, it /p #J-18808-Ljbffr
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