Associate Medical Safety Director

IQVIA UK

Tokyo, Japan
Medical review of aes and adrs
Aggregate safety information review
Medical oversight for label development
This position is a leadership role to manage the Japanese team, reporting globally

Job Summary

  • This position is a leadership role to manage the Japanese team, reporting globally.
  • Responsibilities include providing medical advice on clinical trial or post-marketing safety, evaluating adverse events, and supporting literature reviews, with a focus on antibody drugs, biologics, oncology, and orphan diseases.
  • The role offers full remote work flexibility with a comprehensive benefits package and a structured selection process including an English interview.

Matching Summary

This position is a leadership role to manage the Japanese team, reporting globally.

Skills & Requirements

Must-have

  • Medical review of AEs and ADRs
  • Aggregate safety information review
  • Medical oversight for label development
  • Medical safety review of protocol and IDB
  • Business level English and Japanese proficiency

Nice-to-have

  • Experience in CRO or manufacturer
  • Adaptability in remote environment
  • Leadership and management skills

Key Requirements

  • Japanese medical license
  • Three years clinical practice experience
  • Two additional years in pharmaceutical industry
  • Knowledge of applicable regulations and guidelines
  • Ability to establish and meet priorities and deadlines

Work Rights

Not specified

Tailored Resume

Cover Letter