Senior Medical Writer

What you’d do

Leads development and updates of clinical evaluation reports and post-market surveillance summaries under EU MDR and MEDDEV guidance. Runs systematic literature searches, critically appraises clinical evidence, and prepares literature reviews and benefit-risk assessments for Masimo products. Full time. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• Experience with EU MDR and MEDDEV 2.7/1 Rev. 4
• Systematic literature review and critical appraisal experience
• Managing scientific references and literature search platforms
• Interpreting clinical study protocols and statistical analysis plans
• Summarizing complex clinical information for varied audiences