Technical Editor
Current• Verify preclinical/clinical data within regulatory documents against external source material• Ensure internal data are reported accurately within text and throughout the document• Make nomenclature and terminology consistent, including acronyms, study drug names, etc.• Standardize document content and appearance to client style and formatting guides• Edit body text and tables for grammar, punctuation, spelling, spacing, and number formats• Documents edited include: clinical study reports, informed consent forms, study protocols, investigators’ brochures, briefing books, clinical summaries, nonclinical summaries