Safety Project Mgr（安全性情報管理プロジェクトマネージャー）

IQVIA UK

Tokyo, Japan
Not specified; competitive based on compyny st + a...
4+ years pharmacovigilance experience
Bilingual japanese and english proficiency
Project management in life sciences
The role involves managing pharmaceutical safety information projects across the entire lifecycle from clinical trials to post-marketing while ensuring quality, cost, and delivery targets

Job Summary

  • The role involves managing pharmaceutical safety information projects across the entire lifecycle from clinical trials to post-marketing while ensuring quality, cost, and delivery targets.
  • IQVIA aims to become a trusted strategic partner for customers by providing seamless, visible services through effective oversight of safety teams and global collaboration.
  • Employees benefit from a flexible work style allowing remote work with optional office attendance at Tokyo or Osaka locations, alongside comprehensive welfare benefits.

Matching Summary

The role involves managing pharmaceutical safety information projects across the entire lifecycle from clinical trials to post-marketing while ensuring quality, cost, and delivery targets.

Salary

Not specified; Competitive based on company standards; Annual bonus available

Skills & Requirements

Must-have

  • 4+ years pharmacovigilance experience
  • Bilingual Japanese and English proficiency
  • Project management in life sciences
  • Financial analysis and budgeting skills
  • Risk identification and mitigation strategies

Nice-to-have

  • 2+ years project management experience
  • Experience with PMDA regulatory requirements
  • Global team collaboration skills
  • Process improvement and tool implementation
  • Strong stakeholder relationship building

Key Requirements

  • Bachelor's degree in Life Sciences or related field
  • Minimum 4 years experience in Pharmacovigilance or Medical Information
  • Business-level fluency in both Japanese and English

Work Rights

Not specified

Tailored Resume

Cover Letter