Principal/Head Of Medical Writing

Meet Life Sciences Ltd.; Perugia; On-site; EUR 106,000 - 142,000; Full time

Benefits offered by this job

On-site role

Competitive salary

Job summary

Meet Life Sciences Ltd. is seeking a Principal Medical Writer to lead the development of clinical and regulatory documents for submissions and publications.

You will collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives that support global submissions and impactful communications. You will manage large, complex documentation projects, ensure compliance with regulatory guidelines, and drive innovative writing approaches while maintaining high

Qualifications

• Experience in medical or scientific writing with life sciences focus.
• Knowledge of regulatory guidelines and submission processes.
• Ability to manage large, complex documentation projects.

Responsibilities

• 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.

Skills

Medical writing

Regulatory knowledge

Cross-functional collab

Attention to detail

Communication skills

Education

Life sciences degree

Tools

Document management tools

Job description

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.

• competitive salary package (GBP)
• on-site role
• 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
• 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
• Cross-functional collaboration
• Document management tools and software

Principal/Head of Medical Writing perugia, umbria, it