Medical writer

• Lead the development and execution of medical writing strategies for clinical research projects
• Prepare, review, and edit clinical study protocols, clinical study reports, investigator brochures, regulatory submissions, and other clinical documents
• Collaborate with clinical research, biostatistics, regulatory affairs, and medical affairs teams
• Interpret and analyze clinical trial data and summarize scientific findings
• Participate in planning and execution of clinical development programs
• Provide strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives
• Contribute to publication plans, abstracts, posters, and manuscripts for peer-reviewed journals and scientific conferences
• Mentor and coach junior medical writers on best practices, writing techniques, and scientific principles
• Foster excellence, collaboration, and continuous learning within the medical writing team

Medical writer jobs in North Carolina

Senior Medical Writer