Manager, Regulatory Delivery Excellence, China Regulatory Affairs

Eli Lilly

China
Not specified
Bachelor's degree in pharmaceutical sciences
2+ years drug regulatory affairs experience
Veeva vault rim system expertise
Eli Lilly is seeking a Manager for Regulatory Delivery Excellence in China, responsible for managing regulatory registration processes and submission preparations. The ideal candidate should have a background in pharmaceutical or biopharmaceutical sciences and be equipped with regulatory affairs experience, particularly in leading pharmaceutical companies

Job Summary

  • The role is responsible for managing the full regulatory registration process from clinical trial permits to marketing application withdrawals.
  • Candidates must serve as a Subject Matter Expert for regulatory business processes within the Veeva Vault RIM system.
  • The position requires developing submission plans and collaborating with cross-functional teams including Regulatory TA, CMC, and vendors.

Matching Summary

Match Score: 85

Eli Lilly is seeking a Manager for Regulatory Delivery Excellence in China, responsible for managing regulatory registration processes and submission preparations. The ideal candidate should have a background in pharmaceutical or biopharmaceutical sciences and be equipped with regulatory affairs experience, particularly in leading pharmaceutical companies.

Skills & Requirements

Must-have

  • Bachelor's degree in pharmaceutical sciences
  • 2+ years drug regulatory affairs experience
  • Veeva Vault RIM system expertise
  • Submission dossier compilation skills
  • English writing and speaking proficiency

Nice-to-have

  • Experience leading pharmaceutical company
  • Collaborative relationship building
  • Self-motivated work style
  • Subject matter expert capabilities
  • Vendor management experience

Key Requirements

  • Bachelor's degree required
  • Minimum 2 years experience
  • Pharmaceutical or chemical science background

Work Rights

Not specified

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