Director, Clinical Regulatory Writing

AstraZeneca

Gothenburg, Sweden
Bachelor's degree in life sciences
Significant medical/regulatory writing experience
Expertise in drug development lifecycle
This role leads communications strategy and delivery for the Cardiovascular, Renal and Metabolism (CVRM) portfolio to drive successful submissions and approvals

Job Summary

  • This role leads communications strategy and delivery for the Cardiovascular, Renal and Metabolism (CVRM) portfolio to drive successful submissions and approvals.
  • The Director will act as a visible champion for best practices, innovation, and continuous improvement across the therapy area while mentoring team members.
  • Candidates will join an international, collaborative environment at AstraZeneca's R&D site in Gothenburg to shape standards and grow future leaders.

Matching Summary

This role leads communications strategy and delivery for the Cardiovascular, Renal and Metabolism (CVRM) portfolio to drive successful submissions and approvals.

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences
  • Significant medical/regulatory writing experience
  • Expertise in drug development lifecycle
  • Track record of delivering label-focused documents

Nice-to-have

  • Experience using AI tools for medical writing
  • Strong leadership and coaching abilities
  • Ability to influence stakeholders at highest levels

Key Requirements

  • PhD strongly preferred
  • Proven ability to lead complex submission teams
  • In-depth knowledge of regulatory requirements

Work Rights

Not specified

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