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Pharmacovigilance Reporting Associate

1-3 years
Not Disclosed
10 July 18, 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

 

Pharmacovigilance Reporting Associate – Tokyo

Job Summary:
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Pharmacovigilance Reporting Associate to join its dynamic team in Tokyo. This role focuses on preparing and reviewing safety reports for both clinical trials and post-marketing activities, ensuring full compliance with global regulatory requirements. Ideal for professionals with a background in pharmacovigilance or drug safety, this role provides an excellent opportunity to contribute to global patient safety.


Key Responsibilities:

  • Prepare and review safety reports (e.g., PSURs, ICSRs) in compliance with regulatory standards.

  • Analyze adverse event data from clinical trials and post-marketing surveillance.

  • Ensure timely and accurate submissions to regulatory authorities and sponsors.

  • Collaborate cross-functionally with clinical, regulatory, and data management teams.

  • Stay updated with current pharmacovigilance regulations and industry practices.


Required Skills & Qualifications:

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

  • Prior experience in pharmacovigilance or drug safety.

  • Sound knowledge of regulatory requirements for safety reporting.

  • Strong organizational and attention-to-detail skills.

  • Excellent communication and teamwork abilities.

  • Ability to handle multiple tasks in a fast-paced environment.


Perks & Benefits:

  • Competitive salary (exact figure not specified).

  • Flexible annual leave entitlements.

  • Health insurance options tailored to you and your family.

  • Robust retirement savings and planning support.

  • Global Employee Assistance Programme (LifeWorks).

  • Life assurance coverage.

  • Country-specific benefits: childcare vouchers, bike-to-work schemes, discounted gym memberships, and more.


Company Description:

ICON plc is a global leader in clinical research and healthcare intelligence. With a strong commitment to innovation and diversity, ICON supports biopharmaceutical and medical device companies through every phase of clinical development, prioritizing patient safety and regulatory compliance.


Work Mode: Hybrid or On-site (Tokyo, Japan)
Remote not specified; candidate should be based in or willing to relocate to Tokyo.


Call-to-Action:

If you're passionate about pharmacovigilance and ready to make an impact in global drug safety, apply now to join ICON’s innovative team in Tokyo. Don’t meet every requirement? We still encourage you to apply — your experience may be just what we’re looking for.