On-Site Principal Medical Writer — Regulatory Submissions Lead

Meet Life Sciences Ltd.; Bolzano; On-site; EUR 83,000 - 118,000; Full time

Benefits offered by this job

Competitive salary

On-site role

Job summary

Meet Life Sciences Ltd. is seeking a Principal Medical Writer to lead the development and review of clinical and regulatory documents for submissions and publications. You will translate complex data into clear, regulatory-ready narratives in collaboration with clinical, regulatory, and medical affairs teams.

The on-site role in Bolzano, Italy, rewards expertise and innovation. You will drive high-impact scientific communication, manage large documentation projects, and ensure adherence to

Qualifications

• Extensive experience in medical or scientific writing within life sciences.
• Proven ability to manage large, complex documentation projects.
• Strong understanding of regulatory guidelines and submission processes.
• Excellent communication skills and attention to detail.
• Proficiency with relevant document management tools and software.
• Relevant certifications or advanced degrees in life sciences preferred.

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

Project management

Cross-functional collaboration

Documentation tools

Regulatory submissions

Attention to detail

Communication skills

Life sciences

Data interpretation

Education

Advanced degree in life sciences

Tools

Document management tools

Job description

Meet Life Sciences Ltd. is seeking a Principal Medical Writer to lead the development and review of clinical and regulatory documents for submissions and publications. You will translate complex data into clear, regulatory-ready narratives in collaboration with clinical, regulatory, and medical affairs teams.

The on-site role in Bolzano, Italy, rewards expertise and innovation. You will drive high-impact scientific communication, manage large documentation projects, and ensure adherence to