2008 -2010 Sr. Director Clinical and Regulatory Affairs @
2008 -2008 Head, Regulatory Affairs Central Lab Reagent and Instrument Development, @
2007 -2007 Director Clinical Affairs @
2004 -2007 Director, Clinical and Regulatory Affairs @ Diagnostic Products Corporation, acquired by Siemens Healthcare Diagnostics
1999 -2004 Director Clinical and Regulatory Affairs @ Ischemia Technologies
Deborah Morris Education
New York Medical College
Master of Science (MS) (Biostatistics)
New York University
Master of Science (MS) (Computer Science)
SUNY Albany
Bachelor of Arts (BA) (Biology)
Deborah Morris Skills
FDA
Regulatory Affairs
Quality System
Clinical Research
Medical Devices
Biotechnology
Lifesciences
Validation
Clinical Trials
Infectious Diseases
Hardware Diagnostics
Oncology
Leadership
R&D
GMP
Molecular Biology
Molecular Diagnostics
Cross-functional Team Leadership
Product Development
Biochemistry
Regulatory Requirements
Sop
Data Analysis
ISO
Cardiology
HPLC
ISO 13485
Medical Diagnostics
Microbiology
Strategy
CRO
GCP
GLP
Clinical Development
CAPA
Laboratory
Healthcare
Manufacturing
Quality Assurance
Regulatory Submissions
Commercialization
Quality Auditing
Change Control
Biopharmaceuticals
Product Launch
Immunology
Immunoassays
21 CFR Part 11
Quality Control
Protocol
Microsoft Office
Cross Functional Team Leadership
Program Management
Business Strategy
Research
Business Development
Deborah Morris Summary
Deborah Morris, based in Los Angeles, CA, US, is currently a Principal Consultant at Regulatory and Clinical Affairs Consulting (self employed). Deborah Morris brings experience from previous roles at Cue Health, Regulatory and Clinical Affairs Consulting and Illumina. Deborah Morris holds a Master of Science (MS) in Biostatistics @ New York Medical College. With a robust skill set that includes FDA, Regulatory Affairs, Quality System, Clinical Research, Medical Devices and more. Deborah Morris has 1 emails and 4 mobile phone numbers on RocketReach.
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