
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.
🔥 2 hours ago
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 2 hours ago
Still open on Thermo Fisher Scientific's site. Checked 30 minutes ago.

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.
• Serve as primary author for routine documents such as clinical study reports and study protocols • Summarize data from clinical studies • 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 for assigned deliverables • Represent the department at project launch, review, and project team meetings • Collaborate with internal and external clients to support effective communication and operational excellence
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification • 2+ years of previous experience providing the knowledge, skills, and abilities to perform the job • Experience working in the pharmaceutical/CRO industry preferred • Experience in scientific writing advantageous • Solid medical writing skills, including grammatical, editorial, and proofreading skills • Ability to interpret and present complex data accurately and concisely • Effective administrative, organizational and planning skills; attention to detail and quality • Ability to work on own initiative and effectively within a team • Effective oral and written communication skills • Good knowledge of regulatory documentation and drug development process • Great judgment and decision-making skills • Good computer skills and proficiency with client templates • Good knowledge of document management systems and relevant applications such as Excel and Outlook
• Global team environment • Collaboration and development opportunities • Commitment to scientific excellence • Occasional domestic and international travel
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🕒 March 5
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