ICON Hiring Pharmacovigilance Reporting Associate in Seoul, Korea [High-Paying Jobs 2025]

Apply now for the high-paying Pharmacovigilance Reporting Associate role at ICON in Seoul, Korea. Full-time hybrid job with excellent salary, benefits, and career growth in clinical research and drug safety.

ICON Hiring Pharmacovigilance Reporting Associate in Seoul, Korea [High-Paying Jobs 2025]

ICON plc, a global leader in healthcare intelligence and clinical research, is expanding its pharmacovigilance team with an exciting full-time opportunity for a Pharmacovigilance Reporting Associate in Seoul, Korea. This is an outstanding career opportunity for professionals in clinical research, drug safety, and pharmacovigilance to work with a world-class CRO known for innovation, regulatory excellence, and patient safety.

🌎 About ICON plc – A Global Leader in Clinical Research

ICON plc, headquartered in Dublin, Ireland, operates in over 40 countries, with a workforce exceeding 41,000 employees worldwide. With its focus on clinical development, pharmacovigilance, regulatory compliance, and patient safety, ICON partners with leading pharmaceutical, biotech, and medical device companies to accelerate the development of life-saving therapies.

Key Highlights:

• Industry Leader in Clinical Trials, Drug Safety, and Pharmacovigilance

• Hybrid Work Environment in Seoul, Korea

• Highly Competitive Compensation and Global Benefits

• Cutting-Edge Pharmacovigilance Systems & Processes

📌 Job Overview – Pharmacovigilance Reporting Associate

🎯 Job Responsibilities

As a Pharmacovigilance Reporting Associate, you will play a critical role in ensuring regulatory compliance, patient safety, and accurate safety data reporting:

• Preparation and review of Individual Case Safety Reports (ICSRs), Periodic Safety Update Reports (PSURs), and aggregate safety reports.

• Collection, assessment, and analysis of adverse event data from clinical trials and post-marketing surveillance.

• Continuous monitoring of ICH guidelines, FDA regulations, EMA guidelines, and global regulatory updates.

• Cross-functional collaboration with clinical, regulatory affairs, data management, and medical writing teams.

• Timely submission of safety reports to regulatory authorities and sponsors.

🎓 Eligibility Criteria

Education:

• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields.

Experience:

• Prior experience in pharmacovigilance, drug safety, clinical data management, or regulatory reporting preferred.

• Strong understanding of global pharmacovigilance reporting standards.

Key Skills:

• Meticulous attention to detail with strong analytical capabilities.

• Excellent written and verbal communication.

• Ability to multitask in a regulated, deadline-driven environment.

• Familiarity with MedDRA coding, safety databases, and signal detection tools is an advantage.

💼 Salary & Benefits

ICON offers an industry-leading compensation package aligned with global CRO standards:

• Salary Range: KRW 45–65 million annually (approx. ₹27–₹39 Lakhs INR)*

• Comprehensive Health Insurance coverage for employees and dependents

• Generous Annual Leave and holiday allowances

• Retirement Plans with employer contributions

• Life Assurance and long-term disability coverage

• Employee Assistance Program (EAP) via LifeWorks

• Flexible Benefits: childcare vouchers, gym membership discounts, transportation subsidies

• Hybrid Work Model promoting work-life balance

*Exchange rate approx: 1 KRW = ₹0.06 (for reference)

🌐 Why Choose ICON Korea?

Seoul, Korea has emerged as a global healthcare and biotech innovation hub with over 1,500 growing life sciences jobs. Working with ICON Korea offers:

• Access to cutting-edge clinical research infrastructure

• Professional growth in drug safety, pharmacovigilance, and regulatory affairs

• Collaboration with global pharmaceutical leaders

• Career development through ICON Global Academy Training Programs

🚀 Career Advancement Opportunities

By joining ICON as a Pharmacovigilance Reporting Associate, you open doors to future roles such as:

• Senior Drug Safety Specialist

• Pharmacovigilance Project Manager

• Safety Medical Reviewer

• Regulatory Affairs Manager

• Clinical Operations Lead

ICON’s structured learning and development programs ensure continuous professional growth.

🔒 Fraud Prevention Notice

ICON plc never charges fees for recruitment or applications. Always verify job offers through official ICON platforms. Beware of unsolicited requests for personal or financial information. For inquiries, connect directly via the ICON career portal or contact Jennifer Kim.

📞 How to Apply

Application Process:

• Visit: ICON Careers Portal

• Job Code: JR130553

• Submit required details: first name, last name, email address, and inquiry message.

• Contact: Jennifer Kim via the application portal.

Preparation Tips for Candidates:

• Highlight relevant pharmacovigilance, drug safety, or regulatory compliance experience.

• Demonstrate knowledge of ICH E2B, MedDRA coding, FDA and EMA pharmacovigilance regulations.

• Prepare for interview questions like:

  • “How do you ensure timely and accurate pharmacovigilance reporting?”

  • “What steps do you follow when preparing a PSUR?”

  • “How familiar are you with global regulatory requirements?”

🌟 Join ICON’s Mission to Advance Global Healthcare

At ICON plc, every role contributes to enhancing patient safety and bringing new therapies to market faster. If you are passionate about clinical research, drug safety, and global regulatory compliance, apply now and become part of a diverse global team committed to transforming healthcare.

👉 Apply Today to Start Your Pharmacovigilance Career with ICON in Seoul!