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Pharmacovigilance Reporting Associate Job in Seoul | ICON Careers
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Join ICON as a Pharmacovigilance Reporting Associate in Seoul. Ensure safety report compliance in clinical trials. Apply now for hybrid work and career growth.
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pharmacovigilance reporting associate, drug safety jobs Seoul, PV associate ICON, clinical trial safety reporting, pharmacovigilance jobs Korea, PV compliance, pharmacovigilance hybrid jobs, life sciences jobs Seoul
Job Summary
ICON plc is seeking a detail-oriented Pharmacovigilance Reporting Associate to join their Seoul-based team in a hybrid work model. In this critical role, you will manage the accurate and timely preparation of safety reports for clinical trials and post-marketing activities. You’ll collaborate with multidisciplinary teams ensuring full regulatory compliance, contributing to patient safety and effective drug safety monitoring. This is an excellent opportunity for candidates with a background in life sciences and pharmacovigilance to advance their careers in a world-leading healthcare intelligence company.
Responsibilities
Prepare and review safety reports, including individual case safety reports (ICSRs) and periodic safety update reports (PSURs)
Collect, analyze, and validate adverse event data from clinical trials and post-marketing sources
Ensure compliance with global regulatory pharmacovigilance reporting requirements
Collaborate cross-functionally with clinical, regulatory, and data management teams to resolve reporting issues
Manage timely submission of safety reports to regulatory authorities and sponsors
Maintain up-to-date knowledge of industry guidelines and pharmacovigilance best practices
Support continuous improvement initiatives in safety reporting processes
Required Skills & Qualifications
Bachelor’s degree in life sciences, pharmacy, or a related field
Experience in pharmacovigilance or drug safety reporting
Strong knowledge of pharmacovigilance regulations and safety reporting standards (ICH-GCP, GVP)
Excellent attention to detail and organizational skills
Strong communication and teamwork abilities
Ability to manage multiple tasks and prioritize in a regulated environment
Proficiency with pharmacovigilance databases and Microsoft Office tools is a plus
Perks & Benefits
Competitive salary (specific range not disclosed)
Hybrid work environment offering flexibility
Various annual leave entitlements
Comprehensive health insurance plans for employees and families
Competitive retirement planning and savings programs
Global Employee Assistance Programme (LifeWorks) with 24/7 professional support
Life assurance and flexible country-specific benefits (childcare vouchers, gym discounts, travel subsidies)
Inclusive and diverse workplace culture promoting equal opportunities
About ICON
ICON plc is a global leader in healthcare intelligence and clinical research services, dedicated to advancing drug safety and clinical development. ICON fosters a diverse, innovative work environment focused on compliance, patient safety, and delivering high-quality healthcare solutions worldwide.
Work Mode
Hybrid (Seoul-based office with flexible remote options)
Call to Action
Ready to advance your pharmacovigilance career with a global healthcare leader? Apply now to join ICON as a Pharmacovigilance Reporting Associate in Seoul and help shape the future of clinical drug safety!
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