Senior Medical Writer – Sr. Manager/Associate Director

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Job Description:

  • Develop and lead complex projects, creating comprehensive plans to meet objectives.
  • Collaborate with clinicians, statisticians, and clinical scientists to author protocols and drive document strategies.
  • Independently organize, analyze, and interpret scientific, clinical, and statistical data to prepare key clinical documents.
  • Suggest improvements to document processes or templates to enhance quality and efficiency.
  • Review the work of others in Sub Business Unit/Sub Operating Unit.

Requirements:

  • BA/BS with strong experience or MBA/MS with 5+ years of experience or PhD/JD with some experience or MD/DVM with any years of relevant experience
  • Demonstrated ability to interpret and apply guidelines to document writing, with a comprehensive understanding of the drug development process and regulatory knowledge
  • Excellent project management skills to organize work and handle multiple projects simultaneously
  • Experience with software commonly used to present and analyze data, such as Word, PowerPoint, and Excel
  • Strong analytical and problem-solving skills
  • Exceptional written and verbal communication skills

Benefits:

  • Flexible working hours
  • Professional development opportunities
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