15 ott - Lecce
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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