Medical Writer

Qualifications

• Expertise in Medical Writing and Imaging Endpoints in Trials
• Hands-on Experience with writing imaging charters
• Ability to research and advise on the use of medical imaging endpoints in trials
• Ability to ensure all content complies with relevant regulatory and ethical standards
• Exceptional attention to detail and time management skills
• Advanced degree (e.g., MSc, PhD, or equivalent) in life sciences, medical sciences, or a related field
• Proficiency with medical writing technologies and tools
• Ability to use AI to support you
• Familiarity with drug development processes and clinical trial methodologies

Responsibilities

• Prepare a range of high-quality documents such as imaging charter, site guidelines, reader manuals and other clinical trial documentation
• Participate in development of imaging specifications for product team to support eCRF development
• Understand clinical protocol, specifically imaging sections
• Research and discuss with radiology team about the scoring systems
• Synthesize medical and radiology data
• Ensure all content adheres to regulatory and publication standards
• Collaborate with cross-functional teams, including clinical professionals and project managers