Regulatory Reporting Advisor - Patient Safety

Astrazeneca

Hybrid (minimum of three days per week in-office, with flexibility)
Regulatory documentation & submissions
Literature surveillance
Reportability decisions
AstraZeneca is seeking a Regulatory Reporting Advisor in Patient Safety to ensure timely and compliant regulatory submissions that protect patients. The ideal candidate will have over three years of experience in regulatory affairs or pharmacovigilance, with strong attention to detail and a collaborative approach

Job Summary

  • In this role, you will be a key partner enabling our teams to move faster and deliver with confidence—translating evidence into action that stands up to inspection.
  • Your impact will be felt in every compliant report, every audit-ready trail, and every patient protected.
  • Here, your expertise powers the enterprise—bringing together a diverse set of minds to solve complex problems and accelerate how we safeguard patients.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Regulatory Reporting Advisor in Patient Safety to ensure timely and compliant regulatory submissions that protect patients. The ideal candidate will have over three years of experience in regulatory affairs or pharmacovigilance, with strong attention to detail and a collaborative approach.

Skills & Requirements

Must-have

  • Regulatory Documentation & Submissions
  • Literature Surveillance
  • Reportability Decisions
  • Global Regulatory Standards
  • Pharmacovigilance Reporting

Nice-to-have

  • Cross-functional collaboration
  • Bold thinking
  • Embrace exciting technologies
  • Kindness alongside ambition
  • Curiosity with investment

Key Requirements

  • Bachelor's degree in pharmacy, Life Sciences, Regulatory Affairs, or related field
  • 3+ years of experience in regulatory affairs, pharmacovigilance or regulatory reporting
  • Knowledge of health authority's regulations
  • Good Pharmacovigilance Practice knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter