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ICON plc

Pharmacovigilance Associate

ICON plc

. Monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information .

Posted 10/27/2026full-timeRemote • Poland, BulgariaJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in pharmacovigilance and drug safety, with a strong focus on data analysis, regulatory compliance, and effective communication within cross-functional teams. Maintains up-to-date knowledge of industry regulations and best practices to ensure the safety of pharmaceutical products.

Highest-signal resume keywords
Pharmacovigilance ExperienceAdverse Event ReportingSignal DetectionRegulatory ComplianceAnalytical Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data CollectionRisk AssessmentSafety ReportingRegulatory SubmissionsEvent Processing
Soft Skills
Communication SkillsInterpersonal SkillsAttention to DetailCollaboration
Industry Keywords
Pharmaceutical SafetyClinical EnvironmentQuality StandardsHealthcare DisciplineAdverse Event Analysis

About the role

Key responsibilities & impact
  • Monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information
  • Deliver pharmacovigilance and drug safety work to a high standard
  • Collect and review adverse event reports for accurate and timely reporting in accordance with regulatory guidelines
  • Conduct signal detection and risk assessment activities to identify potential safety issues
  • Collaborate with cross-functional teams on safety-related inquiries and investigations
  • Maintain up-to-date knowledge of pharmacovigilance regulations and industry best practices
  • Assist in preparing safety reports and regulatory submissions

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Experience in pharmacovigilance / drug safety within a clinical or pharmaceutical environment
  • Ability to review and process safety events
  • Strong analytical skills with attention to detail in data collection and reporting
  • Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders
  • Commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities
  • Willingness to travel as required (approximately 10%)
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways