Medical Writing Manager (hybrid)

VRTX (Vertex)

Base: $120,200 - $180,400; bonus/equity: eligible ...
Hybrid
Phd or equivalent degree required
4 years of clinical regulatory writing experience
Authoring clinical study protocols and reports
The role involves preparing moderately complex clinical and regulatory documents such as protocols and study reports under minimal supervision

Job Summary

  • The role involves preparing moderately complex clinical and regulatory documents such as protocols and study reports under minimal supervision.
  • Candidates will serve as the lead Medical Writing Scientist, contributing scientific knowledge to product development plans and ensuring medical consistency across studies.
  • Vertex offers a comprehensive benefits package including medical, dental, vision, generous paid time off, educational assistance, and a hybrid work flexibility option.

Matching Summary

The role involves preparing moderately complex clinical and regulatory documents such as protocols and study reports under minimal supervision.

Salary

Base: $120,200 - $180,400; Bonus/Equity: Eligible for annual bonus and equity awards; Benefits: Inclusive market-leading benefits including PTO and 401(k)

Skills & Requirements

Must-have

  • PhD or equivalent degree required
  • 4 years of clinical regulatory writing experience
  • Authoring clinical study protocols and reports
  • Analyzing and interpreting complex clinical data
  • Managing project teams and cross-functional stakeholders

Nice-to-have

  • Experience with standard operating processes
  • Ability to work resourcefully with minimal supervision
  • Creativity in solving routine problems
  • Strong computer skills for document management

Key Requirements

  • Ph.D. (or equivalent degree)
  • Typically requires 4 years of experience
  • Superior written and oral communication skills

Work Rights

Not specified

Tailored Resume

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