Clario is a global leader in endpoint data solutions for clinical trials, and this role sits within the Medical Imaging team. The Associate Medical Writer will help create and maintain study-specific documentation that supports trial execution, while gaining exposure to clinical research operations, regulatory standards, and imaging science.

• Draft, organize, and curate study startup documents such as Site Manuals, labels, and study-specific forms
• Review protocols and imaging requirements to interpret procedures, schedules, and operational needs accurately
• Create, update, and finalize study documentation, including supporting forms, labels, and communication materials
• Develop compliance artifacts such as Notes to File, amendment impact assessments, and corrective action records
• Prepare meeting agendas, minutes, and action-item logs for study startup and project meetings
• Support document tracking, databases, repositories, and project close-out archiving

• Strong skills in medical writing and clinical trial documentation
• Familiarity with regulatory compliance and medical imaging basics
• Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook
• Excellent attention to detail and proofreading capabilities
• Effective time management and cross-functional collaboration skills

• Work alongside world-class scientists and technologists
• Gain hands-on experience with high-impact clinical studies
• Supportive environment that encourages continuous learning, professional certifications, and global mobility
• Competitive compensation and flexible remote work options
• Clear career roadmap with progression opportunities into Senior Medical Writer, Lead Medical Writer, or Medical Communications Manager