Medical Writer

About the role

MicroPort is seeking a Medical Writer to support its clinical development programs. The role involves preparing clinical study reports, regulatory documents, and a variety of scientific communications with accuracy and clarity.

Key responsibilities

• Collaborate with clinical operations, regulatory affairs and other departments to develop and revise protocols, study reports, investigator brochures and submission materials.
• Write and reference high‑quality manuscripts, slide decks, posters, publications, newsletters and market research reports.
• Conduct literature searches, prepare tables, interpret graphs and perform statistical analyses for assigned communications.
• Support creation of core data sheets, review regional Clinical Evaluation Reports (CERs) and ensure label information is up‑to‑date.
• Organize PMS meetings, analyse product safety data and generate complaint trend reports.
• Search and summarise published clinical data on own and competitor products.

Required profile

• Motivated individual with a strong interest in medical writing and regulatory documentation.
• Ability to work collaboratively across multidisciplinary teams.

Required skills

• Literature search techniques
• Statistical analysis
• Graph interpretation
• Table preparation
• Medical writing for clinical and regulatory contexts

What we offer

• Competitive salary
• Medical insurance covering dental and vision
• Bereavement, maternity and paternity leave
• Paid holidays, seniority days and additional leave options
• Education assistance and professional development opportunities