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  • jobs
  • 2 weeks ago

jobs description

Medical Writing Opportunity with Clinical Research Organization

Responsibilities...
• Critically evaluate, analyze, and interpret medical literature for study design, statistical significance, scientific rigor, and bias absence
• Write and edit various clinical development documents such as clinical protocols, reports, consent forms, and presentation materials
• Meet deadlines, adapt to changes, and maintain workflow for writing assignments
• Provide excellent customer service internally and externally
• Communicate effectively with clients and project team members
• Proactively seek guidance and information from colleagues when needed

Requirements
• Minimum of 3 years of industry or pharma postdoctoral experience
• Masters or Ph.D. in a scientific, medical, or clinical discipline preferred
• Strong understanding of scientific data
• Exceptional writing skills
• Excellent organizational and multitasking abilities
• Proficiency in MS Word, Excel, PowerPoint, and other word processing tools
• Regulatory writing experience and familiarity with client templates and style guides a bonus
• Knowledge of federal regulations, Good Clinical Practices, and ICH guidelines advantageous

If you have a background in medical writing and are looking for a challenging opportunity with a reputable Clinical Research organization, we encourage you to apply for this position.

Employment Type: Full-Time
Canton MI United States

salary-criteria

Apply - Clinical Research Regulatory Medical Writer Canton