Principal Quality Assurance Auditor @ (April 2011 - January 2012)
Sr. Manager, Quality Assurance @ (November 2007 - April 2011)
Lisa Knox Education
California State University - East Bay
B.S. (Health Science)
1994-1996
Lisa Knox Skills
Quality Assurance
Sop
GCP
Clinical Trials
FDA
Quality System
CRO
Clinical Research
Regulatory Affairs
GLP
Pharmaceutical Industry
Biotechnology
Protocol
Software Documentation
Site Inspections
Regulatory Compliance
Good Clinical Practice (GCP)
Regulatory Submissions
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Good Clinical Practice Gcp
Compliance
SAN
Clinical Quality
u.s. Food and Drug Administration Fda
Standard Operating Procedure Sop
Assurance
Standard Operating Procedure
u.s. Food and Drug Administration
Good Clinical Practice
Lisa Knox Summary
Lisa Knox, based in California, United States, is currently a Director, Research and Clinical Development Quality Operations at Alexion/AstraZeneca Rare Disease. Lisa Knox brings experience from previous roles at CytomX Therapeutics, BeiGene, Santen and Dynavax Technologies. Lisa Knox holds a 1994 - 1996 B.S. in Health Science @ California State University - East Bay. With a robust skill set that includes Quality Assurance, Sop, GCP, Clinical Trials, FDA and more. Lisa Knox has 1 emails and 2 mobile phone numbers on RocketReach.
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