Medical Writer

About This Role

This role involves leading and contributing to medical writing projects, focusing on scientific and regulatory documents for clinical development programs. The Medical Writer will collaborate with various teams and clients, ensuring documentation is accurate and compliant, while also acting as a subject matter expert and mentor to junior colleagues.

Responsibilities

• 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
• Support document publishing activities and compilation of submission-ready deliverables
• Manage multiple writing projects simultaneously, ensuring delivery within agreed timelines and budgets
• Track project milestones, risks, and progress using project management tools
• Collaborate closely with project teams, reviewers, and subject matter experts to ensure efficient project execution
• Maintain accurate project records, including time reporting and tracking metrics
• Serve as a point of contact for clients on assigned projects
• Build and maintain strong client relationships through professional communication and high-quality delivery
• Support proposal development, bid defence meetings, and business development activities as required
• Contribute to client satisfaction initiatives and provide feedback to support continuous service improvement
• Provide training, guidance, and mentorship to junior Medical Writers and team members
• Promote knowledge sharing and best practices across the organisation
• Support process improvement initiatives and help drive innovation within the Medical Writing function
• Stay current with evolving regulatory requirements, GCP standards, and scientific communication guidelines
• Share regulatory updates and industry best practices with colleagues and clients
• Engage with relevant industry forums and professional networks to maintain expertise and awareness of emerging trends

Requirements

• Master's degree in Life Sciences, Medical Sciences, Pharmacy, or a related scientific discipline
• 4+ years of medical writing experience within the pharmaceutical, biotechnology, CRO, or healthcare sector
• Strong experience preparing regulatory and scientific documents
• Solid understanding of regulatory requirements and scientific communication guidelines