Associate Director, Regulatory Project Manager
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Lead end-to-end project management of regulatory initiatives and improvement projects (initiation through closure) within budget, scope, and timelines. Oversee regulatory submissions per CSL’s Global Submission Management Process. Manage improvement projects portfolio in alignment with GRA strategy and executive priorities. Mentor junior project managers and support training on submission processes and tools. Requirements Bachelor’s degree in Life Sciences or Business required; advanced degree (MSc, PhD, MBA) and PMP certification preferred. 7+ years of experience in pharma/biotech industry with a focus on biologics and regulatory affairs. 7+ years’ experience managing global, cross-functional projects in a matrix environment. Strong knowledge of global regulatory submission processes, drug development lifecycle, and project governance. Demonstrated success in delivering complex projects on time and within scope. #J-18808-Ljbffr Jobtailor
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