15 ott - Perugia
Meet Life Sciences
Overview As 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 / Benefits * competitive salary package (GBP) * flexible options depending on experience * on-site role * collaborative environment Responsabilità * Lead development and review of clinical and regulatory documents ensuring compliance with industry standards * Manage multiple projects with timelines and deliverables across teams * Build strong working relationships with clinical and regulatory personnel to streamline information flow * Drive innovative approaches to scientific writing for clarity and impact * Analyze and interpret complex data to produce concise documentation * Maintain up-to-date knowledge of regulatory requirements and industry best practices Requisiti fondamentali * Extensive experience in medical or scientific writing within the life sciences * Proven ability to manage large, complex documentation projects * Excellent understanding of regulatory guidelines and submission processes * Strong communication skills and attention to detail * Proficiency with relevant document management tools and software * Relevant certifications or advanced degrees in life sciences are preferred * Strong communication * Attention to detail * Cross-functional collaboration * Document management tools and software
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elettroteammarrinisrls
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