Senior Medical Writer - Clinical Operations
- 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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