Thermo Fisher Scientific
Biotechnology • Pharmaceuticals • Science
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.
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Senior Medical Writer – Client Embedded
Job not on LinkedIn
October 28
Thermo Fisher Scientific
Biotechnology • Pharmaceuticals • Science
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.
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
📋 Description
• Write and edit clinical and regulatory documents • Collaborate with cross-functional teams • Ensure documents align with regulatory guidelines and company standards • 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 • Mentor junior medical writers
🎯 Requirements
• Bachelor's degree in a scientific discipline or equivalent • Advanced degree preferred • Regulatory writing experience (comparable to 5+ years) • Experience working in the pharmaceutical/CRO industry • Experience in managing and directing complex medical writing projects • EU CTR experience preferred
🏖️ Benefits
• Competitive salary • Award-winning learning and development programme • Flexible working culture • Health and well-being benefits
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