Job Summary
A company is looking for a Senior Medical Writer who independently plans and prepares regulatory documents and medical communications to support product development.
Key Responsibilities
- Organize, analyze, interpret, and present scientific and statistical information according to regulatory guidelines
- Collaborate with cross-functional teams for document production
- Prepare a range of regulatory documents to support all phases of product development
Required Qualifications
- Bachelor's degree required; science-related field preferred
- Minimum of 5 years of medical writing experience in a relevant setting, with at least 3 years of formal medical writing experience
- Advanced knowledge of ICH and related regulatory guidelines
- Experience with Microsoft Office Suite, particularly advanced Microsoft Word proficiency
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