Medical Writer – Clinical Evaluation & Regulatory

About the role

Zimmer Biomet is seeking a Medical Writer to develop Clinical Evaluation Reports and post‑market surveillance literature reviews. The role involves systematic searches of peer‑reviewed publications, implant registries and internal risk files to support regulatory submissions and product performance analysis.

Key responsibilities

• Identify and retrieve relevant clinical data from internal and external sources.
• Prepare Clinical Evaluation documents in line with MDR (EU) 2017/745 and company procedures.
• Summarize findings and draft risk‑benefit analyses for senior review.
• Distribute final drafts to Clinical Affairs, Regulatory Affairs, PMS and Engineering for approval.
• Support audit activities as a clinical evidence subject‑matter expert.
• Maintain archives of clinical evaluation work and provide regular progress reports.

Required profile

• Proficient written and spoken English.
• Strong medical and technical writing competence.
• Excellent attention to detail, organization and proofreading abilities.
• Ability to critically analyse and interpret clinical and statistical data.

Required skills

• Medical writing
• Statistical methods