Lead clinical regulatory writing at AstraZeneca in Mississauga, Ontario. This role combines strategic communications with high-quality document authoring to meet regulatory standards and drive efficiency.

AstraZeneca is seeking an Associate Director for its Clinical Regulatory Writing team. In this senior position, you will independently manage writing activities across diverse projects and establish communication standards. Your expertise will contribute to the development of submission strategies while leading teams to ensure timely delivery of critical documents.

Key Responsibilities:
• Manage clinical regulatory writing activities independently
• Author regulatory documents ensuring compliance with quality standards




• Drive development of clinical Submission Communication Strategy
• Lead internal and external authoring teams effectively
• Collaborate proactively at the program level

Requirements:
• Life Sciences degree in a relevant discipline
• 5-9 years of experience in medical/regulatory writing
• Knowledge of drug development processes
• Solid verbal and written English communication skills
• Experience with submission-level authoring

Utilize your communications leadership and regulatory expertise to excel at AstraZeneca.
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📌 Associate Director Clinical Regulatory Writing (Ontario)
🏢 AstraZeneca
📍 Ontario