Medical writer

• Independent authoring, editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports, risk management plans and other documents needed throughout the product’s life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
• Active participation in trainings and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardised documentation
• Support in all pharmacovigilance operations associated with medical writing
• Continuous self-education in all aspects associated with medical writing
• Managing a team of junior medical writers

Medical Writer III

Senior Medical Writer – Line Management Experience Required

Freelance Medical Content Writer

Senior Medical Writer, CTT, Redaction