On-Site Senior Medical Writing Leader

Meet Life Sciences Ltd.; Cagliari; On-site; EUR 83,000 - 106,000; Full time

Job summary

Meet Life Sciences Ltd. in Sardinia invites a Principal Medical Writer to lead the creation and review of clinical and regulatory documents, ensuring clarity and regulatory compliance for global submissions.

You will collaborate with clinical, regulatory and medical affairs teams, manage multiple projects with timelines, mentor junior writers, and drive clear scientific narratives for global regulatory submissions in an on-site, collaborative environment.

Qualifications

• Extensive experience in medical or scientific writing in life sciences.
• Proven ability to manage large, complex documentation projects.
• Excellent understanding of regulatory guidelines and submission processes.
• Strong communication and attention to detail.

Responsibilities

• Lead development and review of clinical and regulatory documents ensuring compliance.
• 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

Lead document development

Project management

Cross-functional collaboration

Regulatory writing

Data interpretation

Regulatory guidelines

Communication skills

Document management

Education

Advanced degree in life sciences

Tools

Document management software

Job description

Meet Life Sciences Ltd. in Sardinia invites a Principal Medical Writer to lead the creation and review of clinical and regulatory documents, ensuring clarity and regulatory compliance for global submissions.

You will collaborate with clinical, regulatory and medical affairs teams, manage multiple projects with timelines, mentor junior writers, and drive clear scientific narratives for global regulatory submissions in an on-site, collaborative environment.