
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.
🔥 36 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts • 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 • 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 • 3+ years of comparable relevant experience • 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 independently and effectively within a team • Effective oral and written communication skills • Good knowledge of regulatory documentation and the drug development process • Good computer skills and proficiency with client templates, document management systems, Excel, Outlook, and other relevant applications • Occasional domestic and international travel and occasional drives to site locations
• Global team environment • Collaboration and development opportunities • Scientific excellence-focused workplace
Apply Now🕒 August 26
Senior Medical Writer developing population PK/PD, CSR, and protocol documents. Supporting ICON’s global healthcare intelligence and clinical research programs.
🕒 April 9
Senior Medical Writer authoring and reviewing regulatory medical writing deliverables for clinical studies. Supporting other writers and undertaking quality control across various domains while adhering to ICH regulations.
🕒 March 29
Medical Writer developing high-quality medical and scientific content aligned with regulatory and brand standards. Supporting Medical Affairs and cross-functional teams in effectively communicating clinical data.
🕒 January 8
Senior Medical Writer managing medical writing activities for Syneos Health. Leading document development and regulatory compliance with a focus on clinical and commercial insights.