Associate Regulatory Affairs Director

AstraZeneca

Hybrid - minimum of three days per week in-office with flexibility.
Extensive regulatory experience in biopharmaceutical industry
Thorough knowledge of drug development lifecycle
Strong project management and leadership skills
AstraZeneca is seeking an Associate Regulatory Affairs Director to lead regulatory submission strategies and ensure that transformative medicines reach patients efficiently. This role requires extensive regulatory experience within the biopharmaceutical industry and strong project management skills, with a focus on collaboration and communication across various teams and regions

Job Summary

  • The Associate Regulatory Affairs Director plays a central role in turning transformative science into approved medicines for patients with unmet medical needs.
  • This position leads end-to-end planning, coordination, and execution of regulatory deliverables while shaping submission strategies and anticipating risks.
  • AstraZeneca fosters an inclusive culture that values diverse perspectives, continuous learning, and smart risk-taking to solve complex challenges.

Matching Summary

Match Score: 85

AstraZeneca is seeking an Associate Regulatory Affairs Director to lead regulatory submission strategies and ensure that transformative medicines reach patients efficiently. This role requires extensive regulatory experience within the biopharmaceutical industry and strong project management skills, with a focus on collaboration and communication across various teams and regions.

Skills & Requirements

Must-have

  • Extensive regulatory experience in biopharmaceutical industry
  • Thorough knowledge of drug development lifecycle
  • Strong project management and leadership skills
  • Experience leading multi-disciplinary project teams
  • Proficiency with MS Project and document management tools

Nice-to-have

  • Managed first wave Marketing Application submissions
  • Knowledge of AstraZeneca business processes
  • Experience managing complex regulatory deliverables
  • Cultural awareness and scientific communication skills
  • Continuous improvement and knowledge sharing focus

Key Requirements

  • Relevant University Degree in Science or related discipline
  • Extensive regulatory experience within the biopharmaceutical industry or health authority
  • Leadership experience managing cross-functional teams

Work Rights

Not specified

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