Senior Medical Writer

Arrowhead Pharmaceuticals, Inc.

San Diego, United States
Base: $100,000—$150,000 usd; bonus/equity: not spe...
On-site
Authoring regulatory documents
Clinical study protocols
Investigator's brochures
The Senior Medical Writer will collaborate with lead medical writers and cross-functional team members to provide authoring support to numerous regulatory documents

Job Summary

  • The Senior Medical Writer will collaborate with lead medical writers and cross-functional team members to provide authoring support to numerous regulatory documents.
  • Responsibilities include contributing author to regulatory documents such as protocols, IBs, CSRs, and components of NDA/MAA documents, and leading author of supporting documents like summary of changes and patient narratives.
  • Arrowhead provides competitive salaries and an excellent benefit package.

Matching Summary

The Senior Medical Writer will collaborate with lead medical writers and cross-functional team members to provide authoring support to numerous regulatory documents.

Salary

Base: $100,000—$150,000 USD; Bonus/Equity: Not specified; Benefits: excellent benefit package

Skills & Requirements

Must-have

  • authoring regulatory documents
  • clinical study protocols
  • investigator's brochures
  • clinical study reports
  • NDA/MAA documents
  • document processes and software

Nice-to-have

  • flexibility and collaboration skills
  • eagerness to learn
  • familiarity with statistical analysis
  • interacting with cross-functional teams

Key Requirements

  • 3 years medical writing experience
  • Bachelor's degree in medically-related field or life science
  • 2 years medical writing experience with Master's or doctoral degree
  • Knowledge of FDA regulations and ICH Guidelines
  • Proficient in MS Word, Excel, EndNote, Adobe Acrobat, PowerPoint

Work Rights

Must have authorization to work in the US

Tailored Resume

Cover Letter