The Lead is a thought leader and subject matter expert on regulatory submission strategies, an energetic communicator equally comfortable at senior governance forums and hands-on training sessions, and a connector who works across functions and TAs to modernize how Sanofi conceives, builds, and delivers regulatory submissions. Serve as the go-to acceleration partner for Global Regulatory Leader and the cross-functional R&D Global Project Team and members across all TAs (CMC, Clinical, Nonclinical, Safety, Commercial, Translational Medicine Unit and Quality colleagues) providing guidance and hands-on support to help them execute faster submissions.