Medical Writer

About the role

As a Medical Writer (Consultant), you will lead and contribute to a variety of medical writing projects, collaborating with cross-functional teams and clients to ensure the delivery of accurate, compliant, and impactful documentation. You will also act as a subject matter expert, providing guidance to colleagues and supporting continuous improvement across the function.

What you'll do

• Medical Writing & Document Development
• Author, review, and quality-check a range of regulatory and scientific documents, including clinical study reports and other medical writing deliverables
• Ensure all documents accurately reflect source data, meet regulatory requirements, and comply with company and client standards
• Manage document review cycles, resolve reviewer comments, and coordinate feedback from multiple stakeholders
• Provide editorial support, proofreading, and quality control reviews where required

What you need

• 4–7 yrs of experience
• CRO
• Communication
• Quality control
• GCP
• Documentation
• M.Sc or M.Pharm or PhD