Keith Weber Location
- New Jersey, United States
Keith Weber Work
- 2023 -now Director @
- 2019 -2023 Associate Director @
- 2015 -2019 Submissions Sr. Publisher and Specialist @
- 2012 -2015 Senior Regulatory Associate @
- 2009 -2011 Submissions Coordinator DRA @
- 2007 -2009 DDMAC Marketed Products Coordinator DRA @
- 2005 -2007 Senior Documentation and Records Specialist @
- 2004 -2005 Regulatory Archiving Specialist @
Keith Weber Education
- RAPS
RAC certification
2019-2019 - Caldwell University
Master of Business Administration - MBA
2017-2019 - Project Management Leadership Group
CPM (Certified Project Manager)
2016-2016 - Montclair State University
BS (Business Administration with a Concentration in Management)
2000-2004
Keith Weber Skills
- Clinical Trials
- eCTD
- Biotechnology
- Regulatory Affairs
- Software Documentation
- Validation
- Quality Assurance
- NDA
- Program Management
- Marketing
- Drug Development
- Clinical Development
- Document Management
- U.S. Food And Drug Administration Fda
- File Management
- Regulatory Submissions
- Electronic Common Technical Document Ectd
- Standard Operating Procedure Sop
- Research
- Pharmaceutical Industry
- FDA
- Sop
- Standard Operating Procedure
- Electronic Common Technical Document
- u.s. Food and Drug Administration
Keith Weber Summary
- Keith Weber, based in New Jersey, United States, is currently a Director at Merck. Keith Weber brings experience from previous roles at Merck, LIQUENT – a PAREXEL Company and Roche Pharmaceuticals. Keith Weber holds a 2019 - 2019 RAC certification @ RAPS. With a robust skill set that includes Clinical Trials, eCTD, Biotechnology, Regulatory Affairs, Software Documentation and more. Keith Weber has 1 emails and 3 mobile phone numbers on RocketReach.
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