Multi-talented Writer well-versed in research, technical writing and editing wide range of content, developing and refining curricula, seeking medical or technical writing position in biotech/pharma industry. Worked with little oversight to write engaging, clean and clear copy and edit technical documents. Proficient in Microsoft Office and Google Docs. Organized and reliable with impeccable grammar and spelling abilities.
• Coordinated and performed the Company’s Quality Control (QC) process for clinical documentation that included but clinical evaluation reports, clinical study reports, patient narratives, and clinical modules for the common technical document.
• Ensured documents comply with Customer templates and style guides.
• Developed and refined training curricula for onboarding medical writers.
• Worked collaboratively with internal and external medical writers, regulatory publishers and project team members to deliver high-quality clinical documentation in a timely manner.
• Promoted development, implementation, and review of editorial management procedures.
• Supported medical writers on the use of tools and technologies to facilitate efficient and compliant document delivery.
• Worked within the document management system, as applicable, to ensure security and version control are maintained.
• Reviewed and edited regulatory documents in multiple therapeutic areas to verify accuracy, completeness, and compliance.