Medical Writer – Medical Information Full Time NEW

Standard (Mon-Fri)

Environmental Conditions

Office

The Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

What You’ll Do:

• May serve as a primary writer who creates and provides input on routine deliverables, such as medical information documents.
• Ensures compliance with applicable SOPs, WI, quality processes, and requirements for documents. May assist in determining best practices for achieving optimal results.
• May assist in program management activities. Duties could include developing timelines and budgets for assigned deliverables and tracking deliverable metrics.

Education & Experience Requirements:

• Bachelor’s degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
• Experience working in the pharmaceutical/CRO industry preferred
• Experience in scientific writing advantageous

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities:

• 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 skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

Working Conditions and Environment:

• Work is performed in an office environment.
• Exposure to electrical office equipment.
• Long, varied hours required occasionally.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.