Medical QC Editor

Roles & Responsibilities
• Review clinical study reports, patient safety narratives, appendices, informed consent forms, clinical protocols, and amendments for accuracy, clarity, and consistency
• Ensure documents align with source data, templates, client requirements, and regulatory standards
• Provide detailed review comments and documentation feedback to Medical Writers
• Complete document reviews and QC checklists within agreed timelines
• Collaborate with writers to resolve discrepancies, omissions, and errors
• Understand assigned tasks and adhere to budgeted hours
• Participate in staff, client, and project update meetings as required
• Review and support updates to departmental templates
• Perform additional duties as assigned by Manager or Supervisor

Qualification
• Associate degree or Bachelor’s degree (B.Pharm/ BS / BA)
• Relevant and equivalent experience may be considered in lieu of formal education

Experience
• Minimum 3 years of clinical research experience
• At least 3 years at Associate Medical QC Editor level

Skills
• Excellent command of written and spoken English
• Strong knowledge of editing and proofreading conventions, grammar, and style
• Understanding of medical, pharmacokinetic, and statistical principles
• High attention to detail and document accuracy
• Knowledge of medical terminology (preferred)
• Proficiency in MS Word, Excel, and PowerPoint

About the Organization
Fortrea – A global clinical development and patient access solutions company delivering high-quality regulatory and clinical documentation, with flexible remote opportunities and strong professional growth in medical writing and quality review.