Be the Voice Behind Life-Changing Science

At Trilogy Writing & Consulting, our medical writers aren’t just writers – they are storytellers who transform data into documents that advance novel therapies.

As a Senior/Principal Medical Writer, you will:

• Produce critical regulatory documents as the lead author for top pharmaceutical clients
• Distill complex study data into logical narratives that compel action
• Manage and coordinate review cycles, timelines, and budgets adeptly
• Provide expert guidance on documentation best practices
• Lead writers to uphold Trilogy’s renowned quality standards
• Help bring new medicines to patients through clinical documents

You have:

• 3-5+ years experience writing regulatory documents as a lead author
• Proven expertise writing protocols, reports, dossiers, publications
• Scientific acumen with sharp attention to detail
• Superior collaboration, project management, and client skills
• Passion for transforming data into stories that change lives

From your home office or our Cambridge/Frankfurt hubs, you’ll enjoy competitive pay, excellent benefits, and career development opportunities.

Join our rapidly growing team of writing experts dedicated to advancing medical science. Apply today!