Ra Specialist Ii_ Project

AbbVie

Hangzhou, China
Not specified; not specified; not specified
Ivdr registration plan execution
New product development project support
Domestic and international clinical coordination
The role involves executing IVDR registration plans to ensure regulatory targets are met on time

Job Summary

  • The role involves executing IVDR registration plans to ensure regulatory targets are met on time.
  • Candidates will act as an RA representative in new product development projects to input regulatory strategies.
  • Responsibilities include coordinating domestic and international clinical matters and assisting with product registration submissions.

Matching Summary

The role involves executing IVDR registration plans to ensure regulatory targets are met on time.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • IVDR registration plan execution
  • New product development project support
  • Domestic and international clinical coordination
  • Product registration submission and renewal
  • Office software proficiency

Nice-to-have

  • Project management certification preferred
  • Hospital clinical practice experience
  • Strong analytical and problem-solving skills
  • Ability to organize internal training sessions
  • High flexibility and proactive attitude

Key Requirements

  • Bachelor's degree or above in medicine, biology, or clinical medicine
  • 1+ years of drug or medical device registration/clinical management experience
  • Good English reading, writing, and speaking skills

Work Rights

Not specified

Tailored Resume

Cover Letter