Quick Overview
Seniority
Mid Senior
Work mode
On Site
Location
Sunnyvale, CA, United States
Posted
Yesterday
Job Description
Key Requirements
- 2 4 years of medical writing experience.
- Experience authoring Clinical Evaluation Reports (CERs) preferred.
- Medical device industry experience strongly preferred.
- Strong knowledge of EU MDR and clinical evaluation requirements.
- Experience with literature searches, systematic literature reviews, critical appraisal, and clinical summaries.
- Experience writing clinical/regulatory documents, protocols, clinical study reports/progress reports, or regulatory submission content.
- Strong scientific/technical writing, editing, proofreading, formatting, and document review skills.
- Ability to manage multiple projects across different surgical/therapeutic areas.
- Strong analytical, organizational, communication, and attention-to-detail skills.
- MD, PhD, or MS in a scientific field preferred.
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