GLP Quality Assurance Auditor @ (January 1998 - January 2002)
Staff Scientist, Drug Metabolism and Pharmacokinetics @ (January 1990 - January 1998)
Clinical Laboratory Director @ Delaware State Hospital (January 1984 - January 1989)
Susan White Education
Salisbury University
BS (Medical Technology)
1976-1980
Wicomico Senior High 1974-1976
Susan White Skills
21 CFR Part 11
Bioanalysis
Biopharmaceuticals
Biotechnology
CRO
CTMS
Clinical Development
Clinical Monitoring
Clinical Operations
Clinical Research
Clinical Study Design
Clinical Trial Management System (CTMS)
Clinical Trials
Collaboration
Compliance
Computer System Validation
Drug Development
Drug Discovery
Drug Metabolism
Drug Safety
EDC
External Audit
External Clients
GCP
GLP
Global Alliances
GxP
ICH-GCP
LIMS
Laboratory
Lifesciences
Medical Affairs
Medical Writing
Pharmaceutical Industry
Pharmacokinetics
Pharmacology
Pharmacovigilance
Protocol
Quality Assurance
Quality Auditing
Quality Management
R&D
Regulatory Affairs
Regulatory Requirements
Regulatory Submissions
SOP
Team Management
Therapeutic Areas
Toxicology
Research
Strategic Planning
Analytics
Computer System
Clinical Trial Management System Ctms
Sales
Project Management
PowerPoint
Ich Gcp
Clinical Trial Management System
Susan White Summary
Susan White, based in Wilmington, DE, US, is currently a Quality Assurance Director, Risk and Analytics at AstraZeneca. Susan White brings experience from previous roles at AstraZeneca and AstraZeneca R&D. Susan White holds a 1976 - 1980 BS in Medical Technology @ Salisbury University. With a robust skill set that includes 21 CFR Part 11, Bioanalysis, Biopharmaceuticals, Biotechnology, CRO and more. Susan White has 3 emails and 3 mobile phone numbers on RocketReach.
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