Thermo Fisher Scientific
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
Senior Medical Writer - EMEA
April 16
Thermo Fisher Scientific
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
📋 Description
• Develop high-quality clinical and regulatory documents ensuring they meet regulatory requirements and company standards. • Collaborate with teams to gather necessary information and ensure document accuracy. • Manage timelines and deliverables for assigned projects. • Ensure documents align with regulatory guidelines and best practices. • Provide feedback on documents prepared by other team members.
🎯 Requirements
• Bachelor's degree in a scientific field or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred. • Regulatory writing experience that provides the knowledge, skills, and abilities to perform the role (comparable to 5+ years). • Experience working in the pharmaceutical/CRO industry required. • Experience in managing and directing complex medical writing projects required. • EU CTR experience preferred. • Experience working on structured content management system and AI-driven content creation, and familiarity with Natural Language Generation preferred.
🏖️ Benefits
• award-winning learning and development programme ensuring you reach your potential. • competitive salary. • extensive benefits package based around health and well-being. • flexible working culture valuing work-life balance.
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