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

IQVIA

Tokyo, Japan
Not specified; annual bonus available; comprehensi...
Pharmacovigilance experience
Japanese and english business fluency
Project planning and budget management
The role involves leading safety information management projects across the entire pharmaceutical lifecycle from clinical trials to post-marketing

Job Summary

  • The role involves leading safety information management projects across the entire pharmaceutical lifecycle from clinical trials to post-marketing.
  • Candidates must possess strong leadership skills to oversee teams and manage customer relationships while ensuring quality, cost, and timeline adherence.
  • The position offers a flexible work style with options for remote work and office attendance at Tokyo or Osaka locations.

Matching Summary

The role involves leading safety information management projects across the entire pharmaceutical lifecycle from clinical trials to post-marketing.

Salary

Not specified; Annual bonus available; Comprehensive benefits including social insurance and company-specific programs

Skills & Requirements

Must-have

  • Pharmacovigilance experience
  • Japanese and English business fluency
  • Project planning and budget management
  • Risk identification and mitigation
  • Stakeholder relationship management

Nice-to-have

  • 2+ years project management experience
  • Matrix organization communication skills
  • Process improvement initiative
  • Customer loyalty and contract renewal focus

Key Requirements

  • 4+ years pharmacovigilance experience in CRO or pharma
  • Bachelor's degree in life sciences or related field
  • Business-level Japanese and English proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter