Senior Vice President, Regulatory Affairs and Quality Assurance @ Nefro Avillion Clinical Development (May 2025 - July 2026)
Vice President, Regulatory Affairs and Quality Assurance @ (January 2021 - May 2025)
Principal Consultant, Regulatory Affairs, Clinical, Quality and Compliance, and Medical Writing @ JEM Biopharma Consulting, LLC (February 2018 - December 2020)
Adjunct Assistant Professor of Regulatory Affairs and Clinical Research and Leadership @ (August 2017 - May 2018)
Vice President, Global Program Management @ (February 2015 - November 2017)
Vice President, Clinical, Quality, and Regulatory Affairs @ (January 2007 - December 2014)
Visiting Scholar @ (January 2006 - May 2007)
Director, Industry Programs @ (January 2003 - January 2007)
Associate Director, Project Management @ (January 2002 - January 2003)
Director, Business Analysis @ (January 2000 - January 2002)
Associate Director, Program Management @ Aronex Pharmaceuticals, Inc. (January 1998 - January 2000)
Medical Writer @ (January 1996 - January 1996)
Jason Moore Education
University of Houston, C.T. Bauer College of Business
M.B.A. (Business Administration)
2000-2001
Texas A&M University
M.S. (Science & Technology Journalism (Medical Writing))
1995-1997
Texas A&M University
B.A. (Psychology)
1985-1990
Jason Moore Skills
GMP
Regulatory Affairs
Lifesciences
GCP
Strategy
Regulatory Submissions
Organizational Leadership
Drug Development
Data Management
General Management
Pharmaceutical Industry
Technology Transfer
Healthcare
CRO
Biotechnology
IND
Clinical Trials
See 20+see Less
Project Management
Public Speaking
Commercialization
Cross Functional Team Leadership
Biopharmaceuticals
EDC
FDA
Oncology
Protocol
Sop
Leadership
Medical Devices
Pharmacovigilance
Research and Development R&d
Change Management
Research
Clinical Development
Good Laboratory Practice Glp
Program Management
Infectious Diseases
Leadership Development
Regulatory Requirements
Quality System
Life Sciences
u.s. Food and Drug Administration Fda
Microsoft Excel
Vaccines
Medical Writing
21 CFR Part 11
Clinical Research
Pharmaceutics
Management
Therapeutic Areas
CRO Management
V&V
CTMS
Validation
u.s. Food and Drug Administration
Good Laboratory Practice
Research and Development
Jason Moore Summary
Jason Moore, based in Salt Lake City, UT, US, is currently a Senior Vice President, Regulatory and Quality at Uniquity Bio. Jason Moore brings experience from previous roles at Nefro Avillion Clinical Development, Avillion Life Sciences, JEM Biopharma Consulting, LLC and The George Washington University School of Medicine and Health Sciences. Jason Moore holds a 2000 - 2001 M.B.A. in Business Administration @ University of Houston, C.T. Bauer College of Business. With a robust skill set that includes GMP, Regulatory Affairs, Lifesciences, GCP, Strategy and more. Jason Moore has 2 mobile phone numbers on RocketReach.
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