Senior Regulatory Medical Writer

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Oversee the entire development process for complex Phase II-IV clinical regulatory documents.

• Engage in strategic meetings to synchronize teams and establish key milestones.

• Facilitate communication strategy meetings and address comments proactively.

• Ensure project goals are consistently aligned across various teams.

• Draft study-level documents, including protocols, lay summaries, and briefing packages.

⛳️ Requirements

• Advanced degree in life sciences, either a PhD or a Master's.

• A minimum of 4 years of experience in regulatory medical writing.

• At least 2 years of experience in a medical writing project lead role.

• Ability to author independently.

• Proactive collaboration with stakeholders is essential.

🏝️ Benefits

• Comprehensive training programs.

• Support from management.

• Opportunities for professional growth and career advancement.