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A leading healthcare organization is seeking an experienced Global Program Regulatory Manager. This hybrid role involves driving regulatory strategy and managing operational activities to support pharmaceutical product development. Candidates should have a background in regulatory affairs, strong understanding of drug development, and relevant degrees. Join a diverse team committed to regulatory excellence in a dynamic environment.
Hybrid: 12 days per month on-site. Location: London (The Westworks), United Kingdom or Dublin, Ireland. Internal Job Title: Global Program Regulatory Manager.
We are looking for an experienced and proactive Regulatory Affairs Manager to join our Global Regulatory Affairs team. This role is critical in driving regulatory strategy and managing operational activities across key regions. You will collaborate with cross-functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and commercialization of pharmaceutical products.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance