Lisa Sauer
Oakland, California, United States
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Lisa Sauer is a highly experienced drug development professional with over 20 years of experience in oncology. She is dedicated to implementing efficient development programs and aggressive regulatory strategies. Lisa is a cross-functional leader who understands the dependencies and needs to work collaboratively. She has a strong background in regulatory affairs, with expertise in clinical trials, clinical development, and post-marketing. Lisa has held various leadership positions at Exelixis, including Vice President of Regulatory Affairs and Quality Assurance. She is based in the United States.
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Successful drug development professional with over 20 years’ experience in oncology. Dedicated to the science and to the patients we serve, with the objective of implementing thoughtful and efficient development programs and aggressive regulatory strategies. A cross-functional leader within drug development, understands the dependencies and need to work together as one team. Often responsible for leading and executing company “firsts” in drug development, is vertically integrated across regulatory disciplines, including clinical development, post-marketing, chemistry, manufacturing and controls (CMC), advertising and promotion, and operations.

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Work Experience

Lisa Sauer's Professional Milestones

  • Manager Regulatory Affairs (2005-08-01~2006-12-01): Drafting and executing successful regulatory strategies to safeguard all intellectual property and ensure compliance.
  • Manager Regulatory Affairs (and Others) (1998-03-01~2005-08-01): Successfully managed multiple regulatory requirements, ensuring compliance and maximizing business governance.
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Education

University of California, Berkeley
University of California, Berkeley

Environmental Economics And Public Policy