Rio Execution Hub Sr. Associate

Pfizer

Hybrid
3+ years professional experience
Advanced to fluent english language
M1 dossier component authoring
The role provides end-to-end management of multi-regional, regional, and national regulatory dossiers for assigned clusters and products

Job Summary

  • The role provides end-to-end management of multi-regional, regional, and national regulatory dossiers for assigned clusters and products.
  • Success is measured by the timeliness, quality, compliance, and efficient delivery of critical on-the-job deliverables.
  • The position partners closely with Country Regulatory Strategists and Hub Submission Managers to enable timely submissions and sustained compliance.

Matching Summary

The role provides end-to-end management of multi-regional, regional, and national regulatory dossiers for assigned clusters and products.

Skills & Requirements

Must-have

  • 3+ years professional experience
  • Advanced to Fluent English language
  • M1 dossier component authoring
  • Local regulatory submission management
  • Quality review of dossier builds

Nice-to-have

  • Multilingual skills desirable
  • Experience with pharmaceutical organizational structures
  • Understanding of country regulatory trends
  • Self-initiated problem solving in ambiguous situations
  • Familiarity with digital transformation strategies

Key Requirements

  • B.S./B.Sc. in Pharmacy, Life Sciences, Business, or IT
  • 3+ years relevant professional experience
  • Advanced Microsoft Office Suite skills

Work Rights

Not specified

Tailored Resume

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