Senior Medical Editor (QC and Regulatory Editing)
- Writing types
- Editing, Regulatory
- Seniority
- Senior
About the role
Responsibilities
- Maintain familiarity with FDA, EU and other relevant guidelines and standards
- Represent the editorial group on study teams and cross-departmental project teams
- Monitor timelines and budgets for assigned projects and escalate risks
- Provide technical support, mentoring and training to medical editing staff
- Serve as project lead for complex or large medical writing deliverables
- Copyedit documents per AMA Manual of Style and custom style guidelines
- Perform quality review of assigned documents for accuracy
- Contribute to process improvement tools and internal editorial policies
- May compile medical writing deliverables
Requirements
- 3-5 years of copyediting experience
- Strong proficiency in Microsoft Word, Excel and PowerPoint
- Knowledge of FDA and EU requirements, ICH regulations and ISO standards
- Excellent attention to detail, accuracy and project management skills
Preferred Qualifications
- Bachelor's degree in life sciences, clinical sciences or English/journalism, or relevant copyediting or quality review experience
- Pharmaceutical, medical device or contract research organization experience
About the Company
Syneos Health is a fully-integrated life sciences services organization supporting drug development and commercialization. Locations listed are Hyderabad and Gurugram, India, with hybrid work.
Listed via Career sites

