Medical writer

• Author, review, and quality check regulatory and pharmacovigilance documents, including PSURs/PBRERs, PADERs, ACOs, DSURs, and Risk Management Plans
• Ensure documents are scientifically accurate, regulatory compliant, and delivered within agreed timelines
• Collaborate with cross-functional teams to analyze, interpret, and present safety data
• Act as a trusted client contact, supporting project delivery and fostering strong working relationships
• Guide, mentor, and share knowledge with junior medical writers
• Contribute to process improvements and enhancement of medical writing quality standards

Explore Medical Writer III, Pharmacovigilance at ERGOMED. Review requirements and application details.