Hybrid Global Regulatory Submissions Lead (CTA/CTR)

Hybrid Global Regulatory Submissions Lead (CTA/CTR)

Full-Time On-site
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Novartis AG in London is seeking a CTA/CTR Team Lead to steer a global regulatory team responsible for high-quality clinical trial submissions and approvals. You will blend people leadership with regulatory expertise to deliver timely outcomes and drive smarter ways of working through simplification and automation.

Based in London with hybrid/remote options for UK-based candidates, the role requires strong regulatory knowledge and international collaboration across teams.

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Hybrid Global Regulatory Submissions Lead (CTA/CTR) employer: Novartis AG

As a Vendor Start-up Manager at our company, you will thrive in a dynamic and supportive work environment that prioritises collaboration and innovation. We offer comprehensive benefits, opportunities for professional growth, and a culture that values your contributions, all while being located in a vibrant area that fosters creativity and connection. Join us to make a meaningful impact in clinical operations and vendor management, where your expertise will be recognised and rewarded.

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Contact Details:

Novartis AG Recruitment Team