Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland.

Overview

As Principal I/II Medical Writer, you will lead regulatory submission activities within a fully remote role across Europe. You’ll work within Syneos Health’s Clinical Solutions, applying deep medical writing expertise to support drug development submissions and regulatory processes. The position emphasizes collaboration, adaptability, and delivering high-quality documentation in a fast-changing environment. This is a chance to shape submissions for innovative therapies while aligning with a mission-driven, inclusive culture.

Pay / Benefits

• career development and progression
• supportive line management
• technical and therapeutic area training
• peer recognition
• total rewards program
• inclusive culture

Responsibilities

• lead/regulatory submission activities
• prepare and contribute to regulatory documentation for submissions
• collaborate with cross-functional teams to understand and shape regulatory needs
• operate in a fast-changing, agile environment to deliver high-quality documents

Key requirements

• regulatory submission experience
• Medical Writer with clinical/submissions background

• collaborative
• agile/adaptable
• problem-solving
• medical writing
• regulatory documentation
• submission planning

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