[innovative Medicine] R&d, Senior Principal Scientist, Pharmacology Group, Preclinical Science &translational Safety Japan

Johnson & Johnson Innovative Medicine

Chiyoda, Tokyo, Japan
Not specified
Nonclinical safety and toxicology expertise
Regulatory submission document preparation
Japanese regulatory requirements knowledge
Johnson & Johnson Innovative Medicine is seeking a Senior Principal Scientist for its Pharmacology Group in Tokyo, Japan. The role focuses on leading nonclinical submissions for regulatory processes and requires extensive experience in toxicology, pharmacology, and DMPK, along with strong communication and leadership skills

Job Summary

  • At Johnson & Johnson, we believe health is everything and strive to innovate across the full spectrum of healthcare solutions to deliver breakthroughs that profoundly impact health for humanity.
  • The role involves ensuring nonclinical studies meet Japanese regulatory requirements and are prepared with high scientific quality using modern approaches including AI.
  • The position requires close collaboration with global teams and external experts to advance drug development pipelines and shape regulatory acceptance aligned with international standards.

Matching Summary

Match Score: 85

Johnson & Johnson Innovative Medicine is seeking a Senior Principal Scientist for its Pharmacology Group in Tokyo, Japan. The role focuses on leading nonclinical submissions for regulatory processes and requires extensive experience in toxicology, pharmacology, and DMPK, along with strong communication and leadership skills.

Skills & Requirements

Must-have

  • Nonclinical safety and toxicology expertise
  • Regulatory submission document preparation
  • Japanese regulatory requirements knowledge
  • Global collaboration and communication
  • Use of AI in document preparation
  • Scientific coaching and mentoring
  • Risk assessment and scientific narrative development

Nice-to-have

  • Advanced presentation and negotiation skills
  • Experience with international regulatory agencies
  • Strategic planning in scientific and regulatory matters
  • Self-management and self-development focus
  • Industry external activity participation

Key Requirements

  • More than 15 years experience in nonclinical areas
  • Expert knowledge in biology, toxicology, pharmacology, and DMPK
  • Advanced knowledge of IND/NDA processes
  • Advanced English communication skills
  • Experience with external industry activities

Work Rights

Not specified

Tailored Resume

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