Clinical Research Associate @ POZEN (January 2008 - May 2008)
Clinical Trial Associate I and II @ (March 2004 - October 2007)
Sarah Silvers Education
University of Southern California
M.S. (Regulatory Science)
Kansas State University
Food Science (elective units)
University of Hawaii at Manoa
BS (Cell and Molecular Biology/ Chemistry)
California State University, Northridge
B.S. (Biology, Chemistry)
College of the Canyons
A.S. (Administration of Justice)
Sarah Silvers Skills
21 CFR Part 11
Biotechnology
CAPA
CRO
CRO Management
CTMS
Clinical Development
Clinical Research
Clinical Trial Management System (CTMS)
Clinical Trials
Compliance
Documentation
EDC
Electronic Data Capture (EDC)
FDA
GCP
Good Clinical Practice (GCP)
Good Laboratory Practice (GLP)
ICH-GCP
Infectious Diseases
Inspection Host
Inspection readiness
Pharmaceutical Industry
Pharmaceuticals
Phase I
Process Validation
Protocol
Quality Assurance
Quality Management System
Quality Systems
Regulatory Affairs
Regulatory Submissions
SOP
Standard Operating Procedure (SOP)
Therapeutic Areas
U.S. Food and Drug Administration (FDA)
Validation
Sarah Silvers Summary
Sarah Silvers, based in San Diego, CA, US, is currently a Head of Clinical QA at Orca Bio. Sarah Silvers brings experience from previous roles at Tenaya Therapeutics, SanBio, Inc. and Catalyst Clinical Research, LLC. Sarah Silvers holds a M.S. in Regulatory Science @ University of Southern California. With a robust skill set that includes 21 CFR Part 11, Biotechnology, CAPA, CRO, CRO Management and more. Sarah Silvers has 2 emails and 2 mobile phone numbers on RocketReach.
Looking for a different Sarah Silvers?
Find contact details for 700 million professionals.