Lead regulatory initiatives at AstraZeneca as the Oncology Regulatory Affairs Director. Use your US regulatory expertise to influence global strategy and ensure timely product approvals.

This senior role at AstraZeneca involves overseeing the regulatory strategy for oncology products. You will support clinical development and lead FDA interactions as part of the Global Regulatory Strategy Team. Your position directly impacts the lifecycle management of creative medicines, making it a critical function within the company.

Key Responsibilities:
• Develop and execute US regulatory strategies for oncology products
• Lead FDA interactions and manage important agency meetings
• Support key regulatory milestones and strategy documents




• Represent US regulatory perspectives in global discussions
• Oversee submissions to maintain compliance and product integrity

Requirements:
• Advanced degree in a scientific discipline
• 10+ years in regulatory affairs within drug development
• Proven experience with EMA and FDA interactions
• Robust communication and collaboration skills
• Demonstrated strategic thinking in regulatory contexts

Position yourself as a key leader in regulatory affairs with AstraZeneca's creative oncology portfolio.
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📌 Oncology Regulatory Affairs Director Role Ontario (Canada)
🏢 AstraZeneca
📍 Canada