About
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.
What you’ll do
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
Who you are
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
Perks
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
MATCH FREE