Pharmacovigilance Scientist 2 (safety Aggregate Report Specialist 2)

IQVIA UK

Not specified
Signal detection and literature lead responsibilities
Authoring pbrers, psurs, dsurs, and acos
4-6 years pharmacovigilance experience required
IQVIA UK is seeking a Pharmacovigilance Scientist 2 to lead signal detection and literature safety surveillance for marketed and investigational products. The role requires expertise in pharmacovigilance, particularly in authoring aggregate reports and managing signal detection activities

Job Summary

  • The role involves acting as a signal detection and literature lead to conduct ongoing safety surveillance for marketed and investigational products.
  • Candidates will be responsible for authoring and finalizing critical aggregate reports including PBRERs, PSURs, DSURs, and ACOs while ensuring compliance with KPIs.
  • The position requires full oversight of molecule deliverables, from signal detection to assessment, and collaboration with cross-functional stakeholders.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Pharmacovigilance Scientist 2 to lead signal detection and literature safety surveillance for marketed and investigational products. The role requires expertise in pharmacovigilance, particularly in authoring aggregate reports and managing signal detection activities.

Skills & Requirements

Must-have

  • Signal detection and literature lead responsibilities
  • Authoring PBRERs, PSURs, DSURs, and ACOs
  • 4-6 years pharmacovigilance experience required

Nice-to-have

  • Excellent written and verbal communication skills
  • Team working capabilities across molecules
  • Experience with regulatory agency inquiries

Key Requirements

  • Life science graduate or pharmacy qualification
  • 4-6 years relevant Pharmacovigilance experience
  • Fluent English spoken and written skills

Work Rights

Not specified

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