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

Collaborate with product development to incorporate new features into client-facing materials.

Provide expert guidance to tech teams, clarifying medical writing needs and workflows.

Collect and analyze user feedback to improve product usability and training programs.

Act as a subject matter expert, staying informed on industry trends and regulatory best practices.

Required Qualifications and Skills

Deep understanding of regulatory medical writing standards and practices (minimum 10 years).

Proven experience in regulatory medical writing, especially CSR development.

Expert knowledge in several additional regulatory document types (e.g., Module 2).

Hands-on mindset with a proactive and goal-oriented approach.

Fluent in English (written and spoken).

Nice-to-have

Interest in the application of AI in medical writing.

Familiarity with AI tools, especially in clinical documentation and regulatory workflows.

Seniority levelDirector

Employment typeContract

Job functionWriting/Editing, Project Management, Customer Service

IndustriesIT System Custom Software Development, Software Development

Note: Removed repetitive location and posting date details to focus on the core job description.

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