Senior Medical Writer

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🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

🏥📝 Medical Writer

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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 medical documents, including Medical Information Response Documents and Questions and Answers. • Research, write, or edit complex clinical, scientific, and program-level documents, including AMCP dossiers and infographics. • Review routine documents prepared by junior team members. • Provide training and mentorship to junior writers on document preparation, software, document types, and therapeutic-area knowledge. • Ensure compliance with quality processes and requirements for assigned documents. • Develop best practices, methods, and techniques for optimal results, including client-specific processes. • Function as a project lead or assist with program management activities. • Develop timelines, budgets, forecasts, and contract modifications; track deliverable metrics; and represent the medical writing team in client meetings. • Collaborate with internal and external clients to support effective and efficient communication and operational excellence.

🎯 Requirements

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic/vocational qualification • Advanced degree preferred • 5+ years of comparable experience providing the knowledge, skills, and abilities to perform the job • Experience working in the pharmaceutical/CRO industry preferred • Additional qualifications in medical writing or medical information advantageous • Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills • Strong project management skills • Excellent interpersonal, problem-solving, negotiation, oral, written, and presentation skills • Significant knowledge of global, regional, national, and other document development guidelines • In-depth knowledge in a specialty area such as preclinical, therapeutic, regulatory submissions, or communications • Strong judgment and decision-making skills • Excellent computer skills and proficiency with client templates • Good knowledge of document management systems and relevant applications such as Excel and Outlook • Occasional ability to drive to site locations and travel domestically and internationally

🏖️ Benefits

• Fully remote work arrangement • Reasonable accommodation for individuals with disabilities during application/interview and employment • Benefits and privileges of employment