Novartis in London is seeking a CTA Submission Manager to steer regulatory activities for clinical trial applications across an assigned portfolio. You will collaborate with study teams, country leads and cross-functional partners to ensure timely, compliant submissions.
The role requires a science degree and at least four years of regulatory experience, with expert knowledge of major country submissions. You will help maintain labeling, safety data interpretation, and contribute to continuous
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Regulatory Submissions Lead – Clinical Trials (Hybrid/Remote) 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.
