Live opening · Posted 7 hours ago

Pharmacovigilance Associate

ICON plc · 2 Locations
Workday
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At a glance

The key details from the original listing.

Posted 7 hours ago
CompanyICON plc
Location2 Locations
SkillsPharmacovigilance
SourceWorkday
ListedPosted 7 hours ago

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About the role

Description supplied by the original job listing.

Pharmacovigilance Associate (Hands-on experience in Clinical Trial & Post Marketing case processing)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Pharmacovigilance Associate at ICON, you will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.
What You Will Be Doing:
Collect, assess, and process adverse event reports to ensure accuracy and timely compliance with regulatory requirements
Partner with cross-functional teams to address safety-related questions and support ongoing investigations
Maintain current knowledge of pharmacovigilance regulations, global safety guidelines, and industry standards
Manage safety inbox and acknowledge case receipt.
Perform case triage and book-in to safety database.
Enter case details accurately and write narratives.
Code events, drugs, and medical history using MedDRA/WHO-DD.
Apply correct product labeling and perform QC checks.
Finalize case processing and generate queries for follow-up
Knowledge of seriousness, expectedness, causality, and global reporting
Familiarity with reconciliation processes and aggregate reporting (PSUR/DSUR)
Ability to mentor new joiners and review SOPs
Working knowledge of SDEA and KPI/SLA basics
Process literature ICSRs and maintain compliance with monitoring requirements
Must Have Criteria:
Minimum 2 years of experience in safety background, with direct involvement in case processing
Solid experience in Post Marketing Surveillance/Clinical Trial case processing
Bachelors degree in life sciences
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
A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
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
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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