Medical Writer
- Writing types
- Regulatory
- Seniority
- Entry
About the role
Responsibilities
- Serve as primary author for clinical study reports, study protocols and clinical data summaries
- Assist with complex clinical, scientific and program-level documents such as IBs, INDs and MAAs
- Ensure compliance with quality processes and requirements for assigned documents
- Assist with timelines, budgets and forecasts for assigned deliverables
- Represent the department at project launch and review meetings
Requirements
- Bachelor's degree in a scientific discipline or equivalent qualification
- Around 2+ years of relevant experience
- Solid medical writing, grammatical, editorial and proofreading skills
- Ability to interpret and present complex data accurately and concisely
- Good knowledge of regulatory documentation and drug development process
- Good computer skills, including Excel and document management systems
Preferred Qualifications
- Experience in the pharmaceutical or CRO industry
- Experience in scientific writing
About the Company
Thermo Fisher Scientific is a global leader in serving science, enabling customers to make the world healthier, cleaner and safer.
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