Medical Writer

Role & responsibilities

• Prepare and review medical, scientific, and clinical documents including:
• Clinical Study Reports (CSRs)
• Protocols and Investigator Brochures
• Regulatory submission documents
• Standard Operating Procedures (SOPs)
• Scientific manuscripts and publications
• Medical education and training materials
• Patient information leaflets and consent forms
• Conduct literature reviews and summarize scientific findings.
• Collaborate with cross-functional teams including Medical Affairs, Clinical Research, Regulatory Affairs, Pharmacovigilance, and Marketing.
• Ensure all documents comply with regulatory and company guidelines.
• Edit and proofread content for clarity, accuracy, consistency, and scientific integrity.
• Support the preparation of presentations, abstracts, posters, and conference materials.
• Maintain document version control and archive records as per compliance requirements.

Preferred candidate profile

• Strong scientific and medical writing skills.
• Excellent written and verbal communication skills in English.
• Ability to interpret and summarize complex scientific data.
• Proficiency in Microsoft Office (Word, PowerPoint, Excel).
• Strong attention to detail and organizational skills.