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Trial Monitoring - System Process Manager (REMOTE)
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.<br><br>We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. <br><br>We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!<br><br>Imagine what you could do here at Novartis!<br><br>This is a Remote based role. Candidates may be located anywhere within the US. <br><br>As a System Process Manager, you will be responsible within the Trial Monitoring Organization for aligning and optimizing systems and related processes to local requirements, including associated project management and the creation, analysis, and presentation of local metrics to inform decision-making processes regarding productivity and effectiveness.<br><br>Major Accountabilities.<br>- Act as a key point of contact for the department, responsible for functionality and customization of clinical trial related IT systems and to independently execute related IT projects<br>- Function as Subject Matter Expert for continuous review of (IT) systems and processes and optimization in terms of simplification, speed, and efficiency<br>- Interdisciplinary exchange with all departments in GDD and Medicine including interface to IT in the context of initiating, coordinating, and executing projects (systems/processes)<br>- Associated change management in the context of implementing new IT systems & processes<br>- Responsible for technical advisement to line functions regarding system capabilities and the impact of process changes on key enterprise data<br>- Creation and analysis of local metrics, KPIs and ad hoc analyses including regular reporting and presentation of business parameters to TMO management and other stakeholders within the communication channels of TMO CT&I<br>- Responsibility for the correctness and completeness of the data in the Clinical Trial Management System including supervision and training of the users and close exchange with the global stakeholders<br>- Independent further development of reporting tools and active participation in global networks that aim to further develop reporting systems, e.g. as an early adopter.<br><br>https://www.youtube.com/watch?v=ggbnzRY9z8w<br>