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Lori Layton Location
Randolph, NJ, US
Lori Layton Work
Associate Director - Global Trial Management @ (June 2010 - Present)
Sr. Clinical Project Manager @ (November 2007 - June 2010)
Trial Manager @ (February 1998 - November 2007)
Lori Layton Education
Bloomsburg University of Pennsylvania
BA
1987-1991
Verona High
Lori Layton Skills
CTMS
Clinical Development
GCP
Clinical Trials
Pharmaceutical Industry
CRO
Regulatory Affairs
EDC
Clinical Research
Clinical Data Management
Drug Development
Clinical Monitoring
Therapeutic Areas
21 CFR Part 11
ICH-GCP
Pharmacovigilance
Oncology
Regulatory Submissions
Sop
GxP
Medical Writing
IND
Clinical Operations
Protocol
Infectious Diseases
Vaccines
FDA
Biotechnology
Diabetes
Cardiovascular
Woman's Health
Ich Gcp
Lori Layton Summary
Lori Layton, based in Randolph, NJ, US, is currently a Associate Director - Global Trial Management at Merck. Lori Layton brings experience from previous roles at Merck and Schering-Plough Research Institute. Lori Layton holds a 1987 - 1991 BA @ Bloomsburg University of Pennsylvania. With a robust skill set that includes CTMS, Clinical Development, GCP, Clinical Trials, Pharmaceutical Industry and more. Lori Layton has 2 emails and 1 mobile phone numbers on RocketReach.
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