Regulatory Reporting Advisor - Patient Safety

Vacancyz

Hybrid (minimum three days per week in the office)
Regulatory documentation & submissions
Pharmacovigilance reporting activities
Assess literature article for reportability
The position of Regulatory Reporting Advisor - Patient Safety at AstraZeneca involves preparing and submitting regulatory reports to ensure compliance with safety standards. The role requires collaboration with cross-functional teams, literature analysis, and a strong understanding of pharmacovigilance practices to protect patient safety

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.
  • We value kindness alongside ambition, and we back curiosity with real investment in learning, so you can grow your impact while helping us move faster, make better decisions, and deliver safety insights that matter.

Matching Summary

Match Score: 85

The position of Regulatory Reporting Advisor - Patient Safety at AstraZeneca involves preparing and submitting regulatory reports to ensure compliance with safety standards. The role requires collaboration with cross-functional teams, literature analysis, and a strong understanding of pharmacovigilance practices to protect patient safety.

Skills & Requirements

Must-have

  • Regulatory Documentation & Submissions
  • Pharmacovigilance reporting activities
  • Assess Literature article for reportability
  • Interpret global regulatory reporting requirements
  • Maintain knowledge of PV regulations

Nice-to-have

  • Cross functional collaborative approach
  • Effective and lateral thinking
  • Vendor management
  • Embrace exciting technologies
  • Kindness alongside ambition

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
  • Pharmacovigilance knowledge excellence
  • Good Pharmacovigilance Practice
  • Knowledge of health authority’s regulations

Work Rights

Not specified

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