Join AstraZeneca in Mississauga as an Associate Director of Clinical Regulatory Writing. This impactful role emphasizes strategic communications and collaboration to enhance regulatory document quality.
In this position, you will lead clinical regulatory writing initiatives within cross-functional teams at AstraZeneca. You are expected to manage writing tasks, establish best practices, and author essential regulatory documents while ensuring adherence to high quality and technical standards. Your contributions will directly influence submission strategies and operational excellence within the organization.
Key Responsibilities:
• Lead clinical regulatory writing activities across various projects • Create and review clinical regulatory documents for quality assurance • Develop clinical Submission Communication Strategy • Collaborate with internal and vendor medical writers • Support team development within Clinical Regulatory Writing
Requirements: • Degree in Life Sciences or relevant field • 5-9 years in medical/regulatory writing • Thorough understanding of drug development • Excellent English communication skills • Proven experience leading teams and authoring submissions
Make a significant impact on regulatory writing efforts with AstraZeneca in Mississauga. #J-18808-Ljbffr