Senior Medical Writer (Sr. Manager/Associate Director)

Overview

In this role, you will lead and execute complex projects in medical writing, collaborating with clinicians, statisticians, and scientists to drive protocol development and document strategy. You will independently analyze clinical, scientific, and statistical data to prepare key clinical documents and identify process improvements. You will review colleagues’ work within the unit, contributing to high-quality, compliant documentation. This position supports Pfizer’s mission to empower better patient care through robust evidence and regulatory-ready submissions.

Pay / Benefits

• remote work
• flexible workplace culture
• global impact
• collaborative environment
• opportunities for career development
• inclusive culture

Responsibilities

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

Key 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
• Ability to interpret and apply guidelines to document writing and understanding of drug development and regulatory processes
• Excellent project management skills for handling multiple projects
• Experience with Word, PowerPoint, and Excel for data presentation and analysis
• Strong analytical and problem-solving skills
• Exceptional written and verbal communication skills

• cross-functional collaboration
• attention to detail
• proactive communication
• Word
• PowerPoint
• Excel

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