2012 -2020 Clinical Research Consultant @ Lisa Vaden, Inc.
2014 -2015 Director Clinical Operations @ Apricus Biosciences, Inc.
2012 -2013 Associate Director @ Lithera, Inc.
2009 -2012 Sr. Clinical Study Manager @ Lithera, Inc.
2009 -2010 Clinical Study Manager @ Lithera
2006 -2009 Sr. Lead Clinical Research Associate @
2000 -2006 Lead Sr. CRA @ Charles River Laboratories
1998 -2006 Lead CRA @ Inveresk
1998 -2006 Sr. Lead Clinical Research Associate @ Charles River Laboratories Clinical Services
1994 -1995 CRA @ Pharmaco LSR
Lisa V. Education
University of Houston
Bachelor of Science (BS)
1986-1990
University of Texas - Health Science Center - Houston
(Public Health)
Lisa V. Skills
CRO
EDC
GCP
Clinical Trials
Clinical Research
Clinical Development
Clinical Monitoring
Oncology
Clinical Trial Management
Biotechnology
ICH-GCP
SOP
FDA
Life Sciences
Dermatology
Ophthalmology
Medical Devices
Endocrinology
Cardiology
Protocol Development
Phase I
PowerPoint
CTMS
Drug Development
Therapeutic Areas
Clinical Research Associates
Protocol
Lifesciences
Clinical Operations
Clinical Data Management
Standard Operating Procedure (SOP)
CRO Management
Electronic Data Capture (EDC)
Clinical Trial Management System (CTMS)
Lisa V. Summary
Lisa V., based in Chula Vista, CA, US, is currently a Sr. Director Clinical Operations at AriBio. Lisa V. brings experience from previous roles at AriBio Co., Ltd., PYC Therapeutics, Spruce Biosciences and Lisa Vaden, Inc.. Lisa V. holds a 1986 - 1990 Bachelor of Science (BS) @ University of Houston. With a robust skill set that includes CRO, EDC, GCP, Clinical Trials, Clinical Research and more. Lisa V. has 3 emails and 1 mobile phone numbers on RocketReach.
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