Sze Lee Email & Phone Number
Associate Director, Clinical Trial Management (Metabolic) @ Kriya Therapeutics, Inc.
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Sze Lee Location
- Chapel Hill, NC, US
Sze Lee Work
- Associate Director, Clinical Trial Management (Metabolic) @ (May 2026 - Present)
- Associate Director, Global Clinical Operations (Ophthalmology) @ (August 2024 - May 2026)
- Sr. Clinical Project Manager (Ophthalmology) @ (January 2023 - August 2024)
- Clinical Project Manager (Ophthalmology) @ (May 2020 - January 2023)
- Clinical Project Manager and Clinical Scientist @ (January 2016 - March 2020)
- Clinical Research Associate @ (January 2014 - December 2015)
- Intern, Regulatory Affairs @ tjun17 Life Sciences (July 2013 - September 2013)
- Translational Research Assistant I and II (Dept. Neuro-Oncology) @ (March 2010 - July 2013)
- Research Assistant (Div. Signal Transduction) @ (June 2008 - February 2010)
- Student Research Intern (Dept. of Biology) @ (September 2007 - May 2008)
- Undergraduate Teaching Assistant (Dept. of Biology) @ (September 2006 - December 2007)
- Summer Intern (Dept. of Cardiovascular and Metabolic Disease) @ (June 2007 - August 2007)
Sze Lee Education
- Northeastern University
Master of Science (M.S.) (Regulatory Affairs for Drugs, Biologics and Medical Devices)
2013-2015 - Brandeis University
B.S. (Biochemistry, Biology)
2004-2008
Sze Lee Skills
- Data Review
- Combination Products
- Diabetes Management
- Neuro-oncology
- Continuous Glucose Monitoring
- Diabetic Retinopathy
- Budget Forecasting
- Budget Tracking
- Mitigation Strategies
- Contract Research Organization (CRO)
- Trial Management
- Gene Therapy
- Scenario Planning
- eCRF
- Ophthalmology
- Interpersonal Skills
- Clinical Research Experience
- Timelines
- Clinical Operations
- Clinical Trials
- Clinical Research
- Regulatory Affairs
- Molecular Biology
- Cell Biology
- FDA
- Tissue Culture
- Biochemistry
- Western Blotting
- Medical Devices
- U.S. Food and Drug Administration (FDA)
- Pharmaceutical Industry
- Good Clinical Practice (GCP)
- Project Management
- IND
- NDA
- Site Selections
- Clinical Site Management
- ICH-GCP
- 510(k)
- IRB submissions
- ISO 14155
- Diabetes
- Vendor Management
- Ich Gcp
- 510K
- Gel Electrophoresis
- Good Clinical Practice Gcp
- Cell
- Scientific Writing
- Sds Page
- U.S. Food And Drug Administration Fda
- Cell Based Assays
- u.s. Food and Drug Administration
- Good Clinical Practice
Sze Lee Summary
- Sze Lee, based in Chapel Hill, NC, US, is currently a Associate Director, Clinical Trial Management (Metabolic) at Kriya Therapeutics, Inc.. Sze Lee brings experience from previous roles at Annexon Biosciences, REGENXBIO Inc. and Senseonics, Incorporated. Sze Lee holds a 2013 - 2015 Master of Science (M.S.) in Regulatory Affairs for Drugs, Biologics and Medical Devices @ Northeastern University. With a robust skill set that includes Data Review, Combination Products, Diabetes Management, Neuro-oncology, Continuous Glucose Monitoring and more. Sze Lee has 1 emails on RocketReach.
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