Full time

Sr. Manager/Associate Director, Regulatory Affairs - CVRM

Posted by AstraZeneca • Daxing District, Beijing, China

📍 Daxing District, Beijing 🕒 March 01, 2026

About the Role

Typical Accountabilities

  • Assist RA TA head to set strategic regulatory direction for China portfolio. to achieve in-time and high-quality approval and facilitate full speed launch, and lead the execution of submission/approval as well as the HA communication.
  • Develop and implement options to deal with changes in timelines and priorities through the comprehensive assessment of various influential factors. Maintain product licenses in assigned portfolio through timely lifecycle management with a high standard.
  • Maintain the awareness of market intelligence and shape the regulatory environment, proactively working on policy interpretation and policy advocacy.
  • Lead the stakeholder management and be good at the complexity management.
  • Supervise, coach, support junior staff, to encourages the sharing of best practices, take decision and accountability for actions; challenge status quo for continuous improvement, help build an open and trusting a...
  • Ready to Apply?

    Submit your application today and take the next step in your career journey with AstraZeneca.

    Apply Now