Peter Karacs
About Peter Karacs
Peter Karacs is a Program Director at Celerion, with extensive experience in clinical operations and project management within the pharmaceutical industry. He has held various roles at notable companies, including Boehringer Ingelheim, Amgen, and ICON Clinical Research, and has a strong academic background in chemistry and accounting.
Current Role at Celerion
Peter Karacs has been serving as a Program Director at Celerion since 2019. In this role, he is responsible for overseeing clinical programs and ensuring the successful execution of clinical trials. His position involves strategic planning and coordination of clinical operations, contributing to the advancement of clinical research within the organization.
Previous Experience in Clinical Research
Peter Karacs has extensive experience in clinical research, having held various positions in notable organizations. He worked at ICON Clinical Research as a Clinical Research Associate (CRA) from 2008 to 2009. He then joined Amgen, where he served as a CRA from 2010 to 2011 and later as a Senior Associate in Clinical Operations Management from 2011 to 2013. His tenure at Boehringer Ingelheim included roles as Regional Clinical Trial Manager and Clinical Trial Information Specialist, among others, from 2013 to 2018.
Educational Background
Peter Karacs has a solid educational foundation in chemistry and business. He studied at Debreceni Egyetem, where he earned a degree in Chemistry from 1996 to 2004. He furthered his education at Budapest University of Technology and Economics, achieving a Master of Science in Analytical Chemistry and Chromatography from 2007 to 2009. Additionally, he studied Accounting at the School of Business from 1998 to 2000.
Career Progression in the Pharmaceutical Sector
Throughout his career, Peter Karacs has progressed through various roles in the pharmaceutical sector, focusing on clinical operations and project management. He worked at Teva Pharmaceuticals as Head of R&D Laboratory from 2004 to 2008 and later at CROMA-PHARMA as a Senior Clinical Project Manager for nine months in 2018. His experience spans multiple key positions that emphasize his expertise in managing clinical trials and improving operational processes.
Skills and Expertise in Clinical Operations
Peter Karacs possesses a strong background in clinical study management, with a focus on improving processes within the pharmaceutical industry. His roles have equipped him with skills in clinical trial management, regulatory compliance, and project coordination. His extensive experience in various capacities has contributed to his proficiency in overseeing complex clinical programs and enhancing operational efficiency.