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 – Early Development Services
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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
• Serve as primary author for routine documents like clinical study reports and study protocols. • Summarize data from clinical studies. • Assist with more complex clinical and scientific documents. • Ensure compliance with quality processes and requirements. • Assist in program management activities, including timelines, budgets, and forecasts. • Represent the department at project launch and review meetings.
🎯 Requirements
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred. • Regulatory writing experience providing 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. • Early phase experience is preferred.
🏖️ Benefits
• award-winning learning and development programme • competitive salary • extensive benefits package based on health and well-being of employees • flexible working culture • work-life balance
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