Principal/Head Of Medical Writing

Altro; Lazio; On-site; EUR 83,000 - 130,000; Full time

Benefits offered by this job

On-site role

Collaborative environment

Job summary

Altro cerca un Principal Medical Writer per guidare la redazione di documenti scientifici per sottomissioni regolatorie e pubblicazioni. Lavorerai a stretto contatto con team clinici, regolatori e medical affairs per trasformare i dati in narrativa chiara.

Il ruolo è on-site in un ambiente collaborativo che valorizza competenze ed innovazione. Contribuirai a migliorare gli outcome dei pazienti a livello globale, definendo approcci di scrittura scientifica e mantenendo allineamento con requisiti

Qualifications

• Extensive experience in medical or scientific writing within life sciences.
• Ability to manage large, complex documentation projects.
• Deep understanding of regulatory guidelines and submissions.
• Strong communication and attention to detail with cross-functional teams.
• Proficiency with document management tools and software.

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

Cross-functional collaboration

Attention to detail

Regulatory understanding

Communication skills

Education

Life sciences degree preferred

Tools

Document management tools

Job description

Overview

Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.

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 xlwpduy 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