安全性情報管理部門スペシャリスト（Pharmacovigilance Specialist）
IQVIA · Tokyo, Japan +1 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This role focuses on pharmacovigilance and safety information management for pharmaceutical and medical device clinical trials and post-market activities. Responsibilities include receiving and processing safety reports, database entry, quality control, regulatory report preparation, signal detection, and periodic safety reporting to regulatory authorities. The position requires 3+ years of case processing experience, Japanese business proficiency, and offers flexible remote work based in Tokyo or Osaka.
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.