Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
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.
Senior Medical Writer – Client Aligned
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
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.
📋 Description
• Write and edit clinical and regulatory documents • Collaborate with cross-functional teams • Ensure documents align with regulatory guidelines and industry best practices • Review documents prepared by team members • Manage timelines and deliverables for projects • Mentor junior medical writers
🎯 Requirements
• Bachelor's degree in a scientific discipline or equivalent • Regulatory writing experience comparable to 5+ years • Experience in the pharmaceutical/CRO industry • Experience in managing complex medical writing projects • EU CTR experience preferred • Excellent organizational and program management skills. • Proven leadership skills to manage and mentor a team of medical writers. • Extensive knowledge of regulatory guidelines and drug development processes. • Strong interpersonal and communication skills. • Understanding of quality control processes.
🏖️ Benefits
• Professional development opportunities
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