MDR – Sr Prin Clinical Research Spec; CER Writer

Responsibilities

• Lead the authoring and critical review of scientific and clinical evaluation documents.
• Analyze complex clinical data into clear, accurate, and defensible written summaries.
• Ensure documents are scientifically sound and consistent.
• Function as a recognized independent SME who can influence decisions.
• Provide strategic clinical input to internal teams and leadership.
• Represent clinical in cross‑functional planning and help the organization understand the clinical implications of decisions.

• Deep clinical research and clinical evidence development experience.
• Expert‑level ability to write, edit, and finalize documents.
• Ability to connect scientific evidence to regulatory, commercial, and clinical needs.
• Exceptional medical writing and scientific communication skills.

Fundamental cardiac knowledge and experience with electrophysiology procedures/technology.