Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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 – FSP
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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 such as clinical study reports and study protocols, and summarize clinical study data • Assist with complex clinical, scientific, and program-level documents, including IBs, INDs, and MAAs • Ensure compliance with quality processes and requirements for assigned documents • Assist in determining best practices, methods, and techniques for optimal results • Assist with program management activities, including developing timelines, budgets, and forecasts • Represent the department at project launch, review, and project team meetings • Collaborate with internal and external clients to support effective communication and operational excellence
🎯 Requirements
• Bachelor's degree in a scientific discipline or equivalent relevant formal academic/vocational qualification • 2+ years of comparable relevant experience • Experience in the pharmaceutical/CRO industry preferred • Experience in scientific writing advantageous • Solid medical writing, grammatical, editorial, and proofreading skills • Ability to interpret and present complex data accurately and concisely • Effective administrative, organizational, and planning skills with attention to detail and quality • Ability to work independently and effectively within a team • Effective oral and written communication skills • Knowledge of regulatory documentation and the drug development process • Judgment and decision-making skills • Good computer skills and proficiency with client templates • Knowledge of document management systems and relevant applications such as Excel and Outlook • Occasional willingness to drive to site locations and travel domestically and internationally
🏖️ Benefits
• Collaboration and development as part of the everyday experience • Reasonable accommodation for individuals with disabilities during application, interview, and employment • Equal opportunity employment
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