2014 -
2014 Research Assistent at Antimicrobial Discovery Center @
2011 -
2013 Genetic Research Assistant @ Henan Key Laboratory of Tumor Epidemiology
2010 -
2013 Clinical Research Assistant @ Key-Disciplines Laboratory Clinical-Medicine
2012 -
2012 Internship in Macromolecule Group @
Shuli Cui Education
Henan University of Technology
Bachelor's Degree
Northeastern University
Master's Degree
Shuli Cui Skills
Clinical Trials
Technical Reviews
Clinical Research
Good Clinical Practice Gcp
Biotechnology
Regulatory Affairs
NDA
Expedited
u.s. Food and Drug Administration Fda
Clinical Operations
Assessment
Regulatory Compliance
EDC
Document Preparation
CMC
Standard Operating Procedure Sop
Science
GLP
Snp
Sop
IVD
Boston
Publications
Approvals
GMP
Sae
English
Validation
Reports
ISO 9001
Strategy
Public Health
Medicine
Testing
Oncology
Risk Management
GCP
Policy
Regulatory Submissions
Informatics
Research
IND
Laboratory
Packet
R
Power
Applications
Bioequivalent
Chinese
Clinical Study Design
Sheets
Scientific
Quality Assurance
Safety
Icf
Marketing
Project
Genetics
RNAi
Odd
Presentations
Batch Records
LinkedIn
ISO 13485
Therapists
Cancer Research
Regulations
Labelling
International
TMF
Reviews
Regulatory
Academic
Materials
Medical Devices
Compliance
Pharmaceutics
China
Biologics
Budgets
Protocol Review
Staff Development
Clarity
Tolerance
DNA extraction
Pharmaceutical Industry
Polymorphism
FDA
Standard Operating Procedure
u.s. Food and Drug Administration
Good Clinical Practice
Shuli Cui Summary
Shuli Cui, based in Boston, MA, US, is currently a Associate Director Regulatory Affairs at Alnylam Pharmaceuticals. Shuli Cui brings experience from previous roles at Alnylam Pharmaceuticals, Karyopharm Therapeutics Inc. and Takeda Oncology. Shuli Cui holds a Bachelor's Degree @ Henan University of Technology. With a robust skill set that includes Clinical Trials, Technical Reviews, Clinical Research, Good Clinical Practice Gcp, Biotechnology and more. Shuli Cui has 2 emails and 1 mobile phone numbers on RocketReach.
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