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Senior Medical Writer
Job Description & How to Apply Below
Syneos Health is hiring a Senior Medical Writer with a specialization in Clinical Trial Transparency. This role demands expertise in regulatory documentation and quality assurance in a cooperative atmosphere.
As a Senior Medical Writer, you will be responsible for authoring rigorous clinical study documents, ensuring quality control, and supporting regulatory submissions. Your collaboration with our Clinical Solutions team will focus on adapting to complex needs while contributing to team mentorship and training processes. This role is key in maintaining the integrity and compliance of clinical documents.
Key Responsibilities:
• Author clinical documents with a focus on quality and compliance
• Execute assignment-specific tasks under defined timelines
• Prepare protocols and disclosure summaries diligently
• Perform quality checks against established benchmarks
• Mentor colleagues based on project requirements
Requirements:
• Significant experience in medical writing and clinical documentation
• Familiarity with clinical trial regulations and guidelines
• Exceptional attention to detail and editing skills
• Strong capability in process analysis and quality assurance
• Engagement in continuous training initiatives
Contribute your expertise to advance clinical trial transparency at Syneos Health.
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Position Requirements
10+ Years
work experience
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