Lisa Grim is a global pharmaceutical program development and compliance leader with a robust history of inspiring cross-functional teams to deliver innovative, compliant, patient-focused solutions. With extensive experience at companies like Teva Pharmaceuticals and Sanofi, Lisa has driven strategic initiatives that enhance operational efficiency and regulatory alignment across the drug development lifecycle. Currently, Lisa serves as a Project Co-Leader at CDISC, focusing on revising the RWE Study Master File to improve usability and adoption, while also pursuing a Bachelor of Science in Management of Technology. Recognized for fostering growth cultures and building trusted partnerships, Lisa embodies a results-oriented approach in navigating complex regulatory environments.
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