Senior Manager/associate Director, Regulatory Affairs - Hematology & Oncology Early Development Ta

Johnson & Johnson UK

Beijing, China
On-site
Regulatory strategy and execution
Hematology/oncology early development
China regulatory interactions
Johnson & Johnson is seeking a Senior Manager/Associate Director in Regulatory Affairs for Hematology & Oncology Early Development in Beijing, China. The role focuses on developing regulatory strategies, managing submissions, and liaising with regulatory agencies to ensure compliance and successful drug development

Job Summary

  • This role is responsible for end-to-end regulatory strategy and execution for new asset development and lifecycle management in Hematology/Oncology early development TA in China.
  • This role will lead China regulatory interactions, drive high-quality submissions and approvals, monitor changes to regulatory requirements and standards, and identify and mitigate regulatory risks.
  • Partner closely with R&D and commercial teams to enable successful drug development, registration and commercial continuity in China.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Manager/Associate Director in Regulatory Affairs for Hematology & Oncology Early Development in Beijing, China. The role focuses on developing regulatory strategies, managing submissions, and liaising with regulatory agencies to ensure compliance and successful drug development.

Skills & Requirements

Must-have

  • regulatory strategy and execution
  • Hematology/Oncology early development
  • China regulatory interactions
  • high-quality submissions and approvals
  • China regulatory agencies liaison

Nice-to-have

  • growth mindset
  • collaboration and influencing skills
  • learning agility

Key Requirements

  • Master’s degree or above
  • More than 5 years of regulatory affairs experience
  • Experience in pharmaceutical R&D
  • Strong familiarity with China regulatory systems

Work Rights

Not specified

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