Director of Regulatory Science @ Camargo Pharmaceutical Services (August 2018 - November 2020)
Sr. Scientific and Regulatory Manager @ Camargo Pharmaceutical Services (January 2016 - July 2018)
Research Scientist 3 @ Camargo Pharmaceutical Services (November 2014 - January 2016)
Research Scientist 2 @ Camargo Pharmaceutical Services (November 2013 - November 2014)
Research Scientist 1 @ Camargo Pharmaceutical Services (April 2012 - November 2013)
Post-doctoral Fellow @ (June 2009 - April 2012)
Graduate Research @ 2005 and 2009 (September 2005 - June 2009)
Undergraduate Research @ Michigan Tech University (January 2004 - April 2005)
Undergraduate Teaching Assistant @ Michigan Tech University (September 2003 - December 2003)
Eric Kendig Education
University of Cincinnati College of Medicine
PhD (Environmental Genetics and Molecular Toxicology)
2005-2009
Michigan Technological University
BS (Biological Science)
2001-2005
Eric Kendig Skills
505 (b)(2)
CRO Management
Drug Development
New Drug Application (NDA)
Pharmaceutical Industry
Pharmaceutics
Research
Research and Development (R&D)
Scientific Writing
U.S. Food and Drug Administration (FDA)
Public Speaking
Cell Culture
u.s. Food and Drug Administration Fda
New Drug Application Nda
Research and Development R&d
Microsoft Word
Services
505 B2
Regulatory
Research and Development
New Drug Application
u.s. Food and Drug Administration
Eric Kendig Summary
Eric Kendig, based in Cincinnati, OH, US, is currently a VP, Regulatory Affairs at MannKind Corporation. Eric Kendig brings experience from previous roles at scPharmaceuticals and Camargo Pharmaceutical Services. Eric Kendig holds a 2005 - 2009 PhD in Environmental Genetics and Molecular Toxicology @ University of Cincinnati College of Medicine. With a robust skill set that includes 505 (b)(2), CRO Management, Drug Development, New Drug Application (NDA), Pharmaceutical Industry and more. Eric Kendig has 3 emails on RocketReach.
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