Associate Director, Pharmacovigilance @ (March 2025 - August 2026)
Senior Manager, Pharmacovigilance, QA @ (April 2024 - March 2025)
Senior Manager, Patient Safety and Pharmacovigilance, Compliance @ (June 2020 - February 2024)
Manager, QMS and GMP Change Control @ (November 2018 - June 2020)
Scientific Project Manager @ (September 2016 - November 2018)
R and D Scientist @ (September 2014 - September 2016)
R and D Scientist @ (January 2007 - September 2014)
Crystal Kim Education
Amberton University
Master of Science (M.S.) (Management/Biomedical Science)
2012-2013
National University of Health Sciences
Bachelor of Science (B.S.) (Biomedical Science)
2011-2012
University of Wisconsin-Madison
Biochemistry
2008-2011
Crystal Kim Skills
Adverse Event Reporting
Analysis
Argus Safety
Audits
Business Continuity Planning
Business Process Improvement
Change Control
Change Management
Clinical Development
Clinical Operations
Clinical Research
Clinical Risk Management
Clinical Trial Management System (CTMS)
Clinical Trials
Compliance
Computer System Validation
Cross-functional Team Leadership
Cultural Sensitivity
Data Entry
Data Integrity
Educational Leadership
FDA GMP
Global Drug Development
Global Health
Global Sourcing
Good Laboratory Practice (GLP)
Good Manufacturing Practice (GMP)
GxP
ICH
Inspections
Internal Audits
International Standards
KPI Reporting
Kidney
Laboratory Automation
Laboratory Equipment
Laboratory Information Management System (LIMS)
Laboratory Medicine
Laboratory Safety
Launch Experience
Leadership
Leadership Development
Learning Management Systems
Management
Managing Associates
Manufacturing
Manufacturing Process Improvement
Mastercontrol
Medical Devices
Microscopy
Microsoft Excel
Microsoft Office
Microsoft Word
Mitigation Strategies
Oracle Database
Organizational Leadership
PADE
PSMF
PV
Pharmaceuticals
Pharmacovigilance
PowerPoint
Presentation Skills
Presentations
Process Improvement
Procurement
Product Development
Product Launch
Program Launch
Project Management
Quality Assurance
Quality Auditing
Quality Control
Quality Management
Quality System
R&D
Recruiting
Regulatory Compliance
Research
Research Project Management
Research and Development (R&D)
Resource Allocation
SOP Authoring
Safety Management Systems
Software Quality Assurance
Standard Operating Procedure (SOP)
Team Building
Team Leadership
Testing
TrackWise
Training
Training Delivery
Training Strategy
Training and Development (HR)
Trial Master File (TMF)
Validation (Drug Manufacture)
Validation Protocol
Veeva Vault
Vendor Management
Verification and Validation (V&V)
Crystal Kim Summary
Crystal Kim, based in Chicago, IL, US, is currently a Director, Pharmacovigilance Compliance and Operational Excellence at Kyverna Therapeutics. Crystal Kim brings experience from previous roles at Thermo Fisher Scientific, Astellas Pharma, Amgen and AmerisourceBergen. Crystal Kim holds a 2012 - 2013 Master of Science (M.S.) in Management/Biomedical Science @ Amberton University. With a robust skill set that includes Adverse Event Reporting, Analysis, Argus Safety, Audits, Business Continuity Planning and more. Crystal Kim has 3 emails and 2 mobile phone numbers on RocketReach.
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