Lisa Freeman's Location
Washington, DC, US
Lisa Freeman's Work
- Executive Director, Regulatory Affairs @ CRISPR Therapeutics
- Senior Director Regulatory Affairs @ REGENXBIO Inc.
- Senior Director, Regulatory Affairs @ Ultragenyx Brasil
- Director, Regulatory Affairs @ MedImmune
- Associate Director, Regulatory Affairs @ MedImmune
- Senior Manager, Regulatory Affairs @ MedImmune
- Manager, Regulatory Affairs @ Nabi Biopharmaceuticals
- Senior Regulatory Project Manager @ GSK
- Regulatory Project Manager @ GSK
- Senior Regulatory Affairs Associate @ GSK
Lisa Freeman's Education
- University of North Carolina at Chapel Hill
Master of Science (M.S.) (Chemistry)
1999 - 2004 - The University of Texas at Austin
Bachelor of Science (B.S.) (Chemistry)
1991 - 1994
Lisa Freeman's Skills
- Regulatory Affairs
- IND
- Biopharmaceuticals
- Regulatory Submissions
- Biologics
- Drug Development
- eCTD
- FDA
- Clinical Trials
- Regulatory Requirements
Lisa Freeman's Summary
Lisa Freeman, based in Washington, DC, US, is currently a Executive Director, Regulatory Affairs at CRISPR Therapeutics, bringing experience from previous roles at REGENXBIO Inc., Ultragenyx Pharmaceutical Inc. and MedImmune. Lisa Freeman holds a 1999 - 2004 Master of Science (M.S.) in Chemistry @ University of North Carolina at Chapel Hill. With a robust skill set that includes Regulatory Affairs, IND, Biopharmaceuticals, Regulatory Submissions, Biologics and more, Lisa Freeman contributes valuable insights to the industry. Lisa Freeman has 5 emails on RocketReach.
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