Manager Clinical Development Quality Assurance, Programs, Biosimilars @ (November 2015 - April 2022)
QC Monitoring Manager @ (April 2014 - October 2015)
GCP Compliance and Training-Support and SOPs Manager @ (July 2012 - March 2014)
Senior CRA Development Manager @ (March 2008 - March 2011)
Associate Director, Clinical Operations @ (April 2006 - February 2008)
CRA Development Manager @ (April 2005 - March 2006)
Senior Clinical Research Associate @ (January 2002 - April 2005)
Clinical Research Associate @ Vujaklija CRO (July 1998 - December 2001)
Istvan Somogyi Education
Technical University
Master of Science, Chemical Engineering
Istvan Somogyi Skills
FDA
Type 2 Diabetes
IRB
Line Management
Pharmaceuticals
Psychiatry
Therapeutic Areas
GCP
Medical Writing
Breast Cancer
Cardiology
Regulatory Affairs
Hypertension
21 CFR Part 11
Clinical Trial
Life Sciences
Clinical
Clinical Trials
Clinical Trial Management
Clinical Monitoring
Cancer
Panic Disorder
CRO
Infectious Diseases
Clinical Data Management
Clinical Research
Site Selections
Asthma
Drug Development
Diabetes
Protocol
Metabolic Diseases
GMP
Oncology
Clinical Development
EDC
CAPA
PowerPoint
JavaScript
Pharmaceutical Industry
Pediatrics
CTMS
Regulatory Submissions
Regulatory Requirements
Lifesciences
Ich Gcp
Sales
Patient Recruitment
Sop
Vaccines
Budgeting
Pharmacovigilance
Istvan Somogyi Summary
Istvan Somogyi, based in Neuenegg, BE, CH, is currently a Evidence Quality Lead (Associate Director) at UCB. Istvan Somogyi brings experience from previous roles at Debiopharm, Formycon AG, Novartis and Grünenthal Group. Istvan Somogyi holds a Master of Science, Chemical Engineering @ Technical University. With a robust skill set that includes FDA, Type 2 Diabetes, IRB, Line Management, Pharmaceuticals and more. Istvan Somogyi has 2 emails on RocketReach.
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