Thermo Fisher Scientific is looking for a Medical Writer to join our team dedicated to a key client in the Functional Service Provider (FSP) space. In this role, you will be responsible for developing high-quality clinical and regulatory documents that meet all regulatory requirements and company standards, enabling customers to make the world healthier, cleaner, and safer.

What You'll Do

Write and edit clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.
Collaborate with cross-functional teams to gather necessary information and ensure the accuracy and completeness of documents.
Ensure documents align with regulatory guidelines, company standards, and industry best practices.
Provide input on document content, structure, and presentation.
Review and provide feedback on documents prepared by other team members.
Manage timelines and deliverables for assigned projects.
Stay current with industry trends, guidelines, and regulatory requirements.

What We're Looking For

Bachelor's degree in a scientific discipline or equivalent and relevant formal academic/vocational qualification.
2+ years regulatory writing experience.
Experience working in the pharmaceutical/CRO industry.

Nice to Have

Advanced degree.
Safety writing experience (e.g. DSUR).
Experience working on structured content management system and AI-driven content creation, and familiarity with Natural Language Generation.

Technical Stack

Structured content management system
AI-driven content creation
Natural Language Generation

Team & Environment

You will be part of the Medical Writing FSP Team. We foster a collaborative environment where teams are eager to share expertise and have fun together, and we value diverse experiences, backgrounds, and perspectives.