Work Schedule Standard Mon-Fri Environmental Conditions Office At Thermo Fisher Scientific you will discover meaningful work that makes a positive impact on a global scale Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future Summarized Purpose We are excited to be expanding our Medical Writing FSP Team in Europe We are looking for a SMW to be dedicated to a client in the FSP space experience in Structured Content Authoring systems and automation to support delivery would be preferred We are seeking a talented and experienced Senior Medical Writer to join our team The Senior Medical Writer will be responsible for developing high-quality clinical and regulatory documents ensuring they meet all regulatory requirements and company standards Key Responsibilities Write and edit clinical and regulatory documents such as 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