Director, Regulatory Affairs

IQVIA

Tokyo, JP
Not specified; annual salary determined by compyny...
8 years regulatory experience
6 years management experience
Line management experience required
The role involves managing staff, overseeing project delivery, and ensuring compliance with strict regulations for biopharmaceutical development

Job Summary

  • The role involves managing staff, overseeing project delivery, and ensuring compliance with strict regulations for biopharmaceutical development.
  • Candidates will support the RADDS Japan initiative to bring emerging biopharmaceuticals to market and assist Japanese ventures in global expansion.
  • The position offers opportunities to contribute to early drug development, engage with cutting-edge therapies like regenerative medicine, and lead complex projects independently.

Matching Summary

The role involves managing staff, overseeing project delivery, and ensuring compliance with strict regulations for biopharmaceutical development.

Salary

Not specified; Annual salary determined by company regulations; Bonus and overtime allowances available

Skills & Requirements

Must-have

  • 8 years regulatory experience
  • 6 years management experience
  • Line management experience required
  • Pharmaceutical or CRO background
  • Strategic regulatory consultancy

Nice-to-have

  • Advanced negotiating skills
  • Conference presentation leadership
  • Bid defense strategy planning
  • Cross-cultural collaboration ability
  • Inspiring vision communication

Key Requirements

  • At least 8 years regulatory experience
  • 6 years of management experience
  • Experience in manufacturer or CRO settings
  • Demonstrated success in senior staff development

Work Rights

Not specified

Tailored Resume

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