Job Title: Associate Director – Clinical Regulatory Writing
Job ID: R-215854
Date Posted: 01/13/2025
Career Level: E
Champion a strategic approach to regulatory decision-making that supports quick, informed choices and balanced risk-taking. As a solution-oriented regulatory expert, you will play a crucial role in shaping drug development earlier in the product lifecycle.
Work at all stages of drug development to turn life-changing science into medicines that make a difference for patients and healthcare professionals worldwide.
At AstraZeneca, we are dedicated to being a Great Place to Work. Our culture champions diversity, collaboration, and lifelong learning, empowering employees to push the boundaries of science.
As a diverse and open-minded regulatory team, we accelerate drug discovery and development. By combining knowledge across therapy areas, we drive rapid, global approvals that bring innovative medicines to patients.
The Clinical Regulatory Writing Associate Director provides strategic leadership and communication expertise for clinical drug programs. This role involves authoring key clinical-regulatory documents, ensuring high-quality standards, and representing regulatory expertise on various projects.
We are committed to innovation and continuous improvement to bring life-changing medicines to patients. Our regulatory approach leads the industry, allowing us to work closely with drug development teams to influence early decisions and drive meaningful contributions throughout the lifecycle of our medicines.
Are you ready to make a difference? Apply now and be part of our mission to push the boundaries of science!
Follow AstraZeneca on LinkedIn: AstraZeneca LinkedIn
AstraZeneca is an equal opportunity employer, committed to diversity and inclusion. We comply with all applicable laws and regulations regarding non-discrimination in employment, work authorization, and employment eligibility verification.
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