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Pharmacovigilance Reporting Associate

3-5 years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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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!