Lisa Grim is a global pharmaceutical program development and compliance leader recognized for inspiring cross-functional teams to deliver innovative, patient-focused solutions. They served in various leadership roles at Sanofi and Teva Pharmaceuticals, where they drove strategic initiatives, managed complex regulatory environments, and championed organizational change. Currently, Lisa co-leads the RWE Study Master File 2.0 project at the Clinical Data Interchange Standards Consortium (CDISC), enhancing usability and collaboration across global teams. Additionally, they are pursuing a Bachelor of Science in Management of Technology at Kennedy Western University.
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