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Manager, Pharmacovigilance

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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Meta Title:
Manager Pharmacovigilance Job Tokyo | ICON Drug Safety Role

Meta Description:
Apply for Manager Pharmacovigilance at ICON Tokyo. Lead drug safety operations, ensure compliance, and drive risk management in clinical trials. Join now!

Meta Keywords:
pharmacovigilance manager Tokyo, drug safety manager job, clinical safety monitoring, pharmacovigilance jobs Japan, drug safety compliance, clinical research pharmacovigilance, ICON pharma jobs, safety data management


Job Summary

ICON plc is seeking a skilled Manager, Pharmacovigilance to lead drug safety operations in Tokyo. This role is ideal for pharma professionals with extensive experience in pharmacovigilance, regulatory compliance, and risk management within clinical research. As the pharmacovigilance lead, you will manage safety reporting, develop policies, and collaborate cross-functionally to ensure patient safety and regulatory adherence throughout clinical trials.


Responsibilities

  • Lead and manage the pharmacovigilance team to ensure timely and accurate adverse event reporting.

  • Develop and implement pharmacovigilance policies and risk management procedures.

  • Collaborate with clinical operations and regulatory teams to integrate safety data into development plans.

  • Monitor and analyze safety data trends to identify potential risks and support clinical trial decisions.

  • Stay current with global pharmacovigilance regulations and best practices to drive continuous improvements.


Required Skills & Qualifications

  • Degree in life sciences, pharmacy, or related field; advanced degree or certifications preferred.

  • Significant experience in pharmacovigilance or drug safety within pharmaceutical or clinical research sectors.

  • Strong knowledge of regulatory requirements for drug safety and safety reporting.

  • Excellent analytical, problem-solving, and data-driven decision-making skills.

  • Effective communication and interpersonal skills to influence diverse stakeholders.


Perks & Benefits

  • Competitive salary (compensation range not specified).

  • Various annual leave entitlements.

  • Comprehensive health insurance plans for employees and families.

  • Competitive retirement planning options.

  • Global Employee Assistance Program (LifeWorks) offering 24/7 support.

  • Life assurance coverage.

  • Flexible country-specific benefits such as childcare vouchers, gym memberships, bike schemes, and subsidized travel passes.


Company Description

ICON plc is a global leader in clinical research and healthcare intelligence, dedicated to innovation and fostering an inclusive culture. ICON delivers cutting-edge clinical trial solutions that improve patient outcomes worldwide.


Work Mode

On-site — Tokyo, Japan


Call to Action

Ready to lead pharmacovigilance activities at a world-class clinical research organization? Apply now to become a Manager, Pharmacovigilance at ICON Tokyo and contribute to advancing global drug safety and patient care!