Medical Writer (FSP) - Client Aligned

Thermo Fisher Scientific · Remote

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Medical AffairsRemoteFull timeCompany career page

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Role summary

Thermo Fisher Scientific seeks an experienced medical writer for a dedicated client role within their FSP team in Spain. The position involves developing clinical and regulatory documents while ensuring compliance with regulatory standards and industry best practices.

What they're looking for

Bachelor's degree in scientific discipline or equivalent; advanced degree preferred
3+ years of regulatory writing experience in pharmaceutical or CRO industry
Knowledge of regulatory guidelines and drug development processes
EU CTR experience preferred
Strong organizational, communication, and interpersonal skills
Experience with structured content authoring systems and automation preferred

What you'll be doing

Write and edit clinical study reports, protocols, investigator brochures, and regulatory submissions
Collaborate with cross-functional teams to gather information and verify document accuracy
Ensure compliance with regulatory guidelines, company standards, and industry best practices
Manage project timelines and deliverables
Monitor regulatory requirements and industry trends

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Date posted3 days ago

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