
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.
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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.
• Develop project timelines, standards, budgets, and forecasts • Collaborate with cross-functional teams to meet deliverables • Monitor timelines and provide status updates • Identify and resolve client management issues • Ensure compliance with quality processes • Lead initiatives involving Informed Consent Forms (ICFs) and other critical clinical research documents • Deliver high-quality, compliant medical writing project outputs
• Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience • Experience managing medical writing or clinical projects • Pharmaceutical/CRO industry experience preferred • Experience in regulatory and/or plain language medical writing advantageous • Proven project management skills • Strong planning and organizational abilities • Excellent interpersonal and communication skills • Ability to work independently and under pressure • Solid project management, budgeting, and forecasting skills • Effective problem-solving and decision-making abilities • Proficient in global and regional regulatory guidelines
• Competitive remuneration • Annual incentive plan bonus • Healthcare • Range of employee benefits • Career and development prospects • Innovative, forward-thinking organization • Exciting company culture centered on integrity, intensity, involvement, and innovation
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