Submission Readiness Document Manager

Experteer Overview
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In this role you ensure clinical documents are submission-ready and technically compliant to drive timely regulatory submissions. You work with global teams to strengthen document management processes and standards, enabling regulatory success. You’ll lead editorial, formatting, and templating efforts while tracking risks and driving improvements in a fast-paced environment. You’ll collaborate across functions to deliver high-quality documents and support audits, with a clear focus on data integrity and regulatory guidelines. This is an opportunity to shape how clinical documentation supports patient access to medicines at Novartis.
Compensaciones / Beneficios
• Manage submission-readiness of clinical documents ensuring regulatory compliance and quality
• Oversee technical editorial and formatting for regulatory submissions
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