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Senior Medical Writer - Clinical Operations

Convatec · London, GB

Writing types
Regulatory, Scientific communications
Seniority
Senior

About the role

Responsibilities

  • Develop protocols, study reports, and clinical investigation materials across Convatec Business Units
  • Prepare data summaries for internal teams, HCPs, patients, and regulatory authorities
  • Implement Good Clinical Practice in all clinical study documents
  • Perform literature searches and reviews to support study design and strategic decisions
  • Stay current on registered studies and published literature in relevant therapy areas

Requirements

  • BSc with 7-10 years relevant experience, or MSc with 3-5 years, or PhD
  • Experience writing clinical study documents
  • Trained in Good Clinical Practice
  • Excellent written communication skills
  • Good working knowledge of Embase and PubMed

Preferred Qualifications

  • Knowledge of CTMS and eTMF
  • Knowledge of medical device or pharmaceutical industry

About the Company

Convatec is a global medical products and technologies company focused on chronic condition management, with leading positions in advanced wound care, ostomy care, continence and critical care, and infusion care.

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