Lay Language Medical Writer

Position: Lay Language Medical Writer - Contract Lay Language Medical Writer – Freelance / Contract - 6 month contractLocation: Remote – Europe or US East Coast preferredEmployment Type: Freelance / Independent ContractorHours: Flexible, 5 hours up to 35 hours per week - 6 month contractIndustry: Pharmaceuticals / Clinical ResearchAL Solutions is partnering with a global life sciences organisation to recruit an experienced Lay Language Medical Writer for a flexible, remote consulting opportunity.We are seeking a specialist with extensive experience developing, reviewing and editing Lay Summaries of Trial Results (STRs), ensuring complex clinical trial information is communicated clearly and accurately to non-scientific audiences.This opportunity would suit an established freelance medical writer looking to support international clinical research programmes on a flexible, project-based basis.Key Responsibilities Lead the development and authoring of Lay Summaries of Trial Results (STRs).Translate complex clinical trial data into clear, accurate and accessible language for patients and the general public.Conduct quality control (QC), editing and review of lay language documents.Collaborate with cross-functional clinical, regulatory and medical writing teams.Ensure documents meet applicable regulatory requirements, quality standards and project timelines.Utilise Please Review for document development, review and quality control.Work collaboratively with stakeholders across Europe and the Eastern United States.Extensive professional experience in medical writing within the pharmaceutical, biotechnology or CRO industry.Lead Author experience on a minimum of 5 Lay Summaries of Trial Results (STRs).Quality Control experience on at least 2 STR documents.Editing experience on at least 2 STR documents.Demonstrable expertise in communicating complex scientific and clinical information to non-specialist audiences.A terminal academic degree in a relevant scientific or medical discipline, with a PhD preferred.Excellent written English, attention to detail and ability to work independently.Ability to accommodate some collaboration with teams operating in European and US Eastern time zones.Experience preparing Lay Protocol Synopses, Lay Informed Consent Forms or other patient-facing clinical trial documentation.Familiarity with clinical trial transparency and disclosure requirements.Previous experience working with global pharmaceutical companies or CROs.Experience using Please Review or similar collaborative document review platforms.Working arrangement: Fully remote.Commitment: Approximately 5 hours per week initially, with additional writing assignments scoped and budgeted individually.Working hours: Flexible, with some availability towards the end of the US Eastern Time working day.Equipment: Consultants must provide their own equipment, meeting relevant IT and security requirements.Onboarding: Project-specific training will be provided, with agreed training time billable.Why Apply?This is an excellent opportunity to contribute to international clinical research programmes while maintaining the flexibility of independent consulting.You will work with experienced global teams on scientifically important projects, helping make clinical trial results more accessible and understandable to patients and the wider public.Applications will be reviewed based on relevant STR experience.