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Job Description & How to Apply Below
This role requires a strong grasp of FDA and EU regulations to ensure that all documents produced exceed quality standards. You'll work closely with cross-departmental teams to deliver complex projects while mentoring medical writing staff.
Your role also emphasizes maintaining budgets, timelines, and providing editorial guidance throughout the project lifecycle.
Key Responsibilities:
• Oversee the editing of documents for regulatory compliance
• Represent editorial needs in various project teams
• Conduct training sessions for medical writing staff
• Facilitate project meetings and distribute necessary information
• Ensure timely and budget-friendly project completions
Requirements:
• Proven proficiency in medical writing and editing
• Deep understanding of regulatory guidelines
• Exceptional attention to detail in grammar and style
• Leadership ability to mentor writing teams
• Experience in managing project timelines and budgets
Apply your expertise to improve patient outcomes at Syneos Health.
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Position Requirements
10+ Years
work experience
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