Senior Medical Writer

TriloDocs Ltd; London; Remote; GBP 60,000 - 90,000; Full time

Job summary

Une entreprise innovante dans le domaine de l'écriture médicale recherche un rédacteur médical réglementaire expérimenté pour un rôle de conseil. Vous travaillerez à distance avec les équipes produit et techniques pour affiner des solutions logicielles alimentées par l'IA, garantissant la satisfaction des clients et influençant le développement de l'offre de produits et services.

Qualifications

• Compréhension approfondie des normes de rédaction médicale réglementaire (minimum 10 ans).
• Expérience prouvée en rédaction médicale réglementaire, notamment dans le développement de CSR.
• Connaissance experte de plusieurs types de documents réglementaires.

Responsibilities

• Collaborer avec le développement produit pour intégrer de nouvelles fonctionnalités.
• Fournir des conseils d'expert aux équipes techniques sur les besoins en rédaction médicale.
• Analyser les retours utilisateurs pour améliorer l'utilisabilité du produit.

Skills

Rédaction médicale réglementaire

Analyse des retours utilisateurs

Connaissance des normes réglementaires

Communication en anglais

Job description

Advisory Role – TriloDocs (Remote)

Help shape the future of AI-driven medical writing.

About TriloDocs

TriloDocs is an AI-powered tool designed to generate the initial draft of Clinical Study Reports (CSRs), streamlining the regulatory writing process.

About the Role

We are seeking an experienced regulatory medical writer to join TriloDocs in an advisory capacity. In this remote role, you will work closely with our product and tech teams to refine and build AI-powered software solutions tailored to the needs of regulatory medical writing professionals. Your insights will help ensure client satisfaction and shape the development of our product and service offering.

Key Responsibilities

1. Collaborate with product development to incorporate new features into client-facing materials.
2. Provide expert guidance to tech teams, clarifying medical writing needs and workflows.
3. Collect and analyze user feedback to improve product usability and training programs.
4. Act as a subject matter expert, staying informed on industry trends and regulatory best practices.

Required Qualifications and Skills

1. Deep understanding of regulatory medical writing standards and practices (minimum 10 years).
2. Proven experience in regulatory medical writing, especially CSR development.
3. Expert knowledge in several additional regulatory document types (e.g., Module 2).
4. Hands-on mindset with a proactive and goal-oriented approach.
5. Fluent in English (written and spoken).

Nice-to-have

1. Interest in the application of AI in medical writing.
2. Familiarity with AI tools, especially in clinical documentation and regulatory workflows.

Seniority level

Director

Employment type

Contract

Job function

Writing/Editing, Project Management, Customer Service

Industries

IT System Custom Software Development, Software Development

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