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.
Responsibilities
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
Requirements
~ 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

📌 Medical Writer (España)
🏢 Thermo Fisher Scientific
📍 España