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 projectsCreate and review clinical regulatory documents for quality assuranceDevelop clinical Submission Communication StrategyCollaborate with internal and vendor medical writersSupport team development within Clinical Regulatory WritingRequirements:Degree in Life Sciences or relevant field5-9 years in medical/regulatory writingThorough understanding of drug developmentExcellent English communication skillsProven experience leading teams and authoring submissionsMake a significant impact on regulatory writing efforts with AstraZeneca in Mississauga.#J-18808-Ljbffr