One of Insight Global's largest pharmaceutical clients is looking for someone to join their Global Regulatory Affairs organization and Regulatory Information Management team to support various change management initiatives, including managing a suite of documentation that supports regulatory processes and transforming this documentation with the use of the Veeva platform. This individual will sit remotely and be responsible for Providing Change Management, Communication and Training support for system-related initiatives across HRM (Health Registration Management). They will be responsible for supporting all regulatory processes as they relate to HRM and its systems, including Labeling, CMC, Commitments, Clinical Trial Applications, Investigational New Drugs, Publishing and Planning, and Medical Device Combination Products.. Support development and execution of change management, communication, and training plans. Partner with stakeholders to draft and distribute project communications and end user support materials, including but not limited to newsletters, SharePoint sites, user guides, PowerPoint presentations, animated videos, etc.

This role is fully remote and only offers 30 total hours of work per week.

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