Adrienne Stadler
About Adrienne Stadler
Adrienne Stadler is a Quality Manager and Regulatory Affairs Manager with extensive experience in clinical project leadership. She has worked at Celerion since 2015 and previously held positions at Assign Group from 2006 to 2015.
Work at Celerion
Adrienne Stadler has been employed at Celerion since 2015, where she holds the positions of Quality Manager and Regulatory Affairs Manager. In these roles, she is responsible for overseeing quality assurance processes and ensuring compliance with regulatory standards. Her tenure at Celerion has lasted for 9 years, during which she has contributed to maintaining high-quality standards in clinical research and development.
Previous Experience at Assign Group
Prior to her current role, Adrienne Stadler worked at Assign Group from 2006 to 2015. Initially, she served as a Clinical Project Manager for one month in 2006. Following this brief period, she took on the role of Clinical Project Leader, where she worked for 8 years until 2015. Her experience at Assign Group involved managing clinical projects and ensuring adherence to project timelines and objectives.
Education and Expertise
Adrienne Stadler earned her Bachelor of Science degree from the Dyson School of Design Engineering, where she studied from 1997 to 2001. This educational background has provided her with a solid foundation in design engineering principles, which she applies in her roles in quality management and regulatory affairs.
Career Overview
Adrienne Stadler has built a career in quality management and regulatory affairs, with significant experience in clinical project management. Her professional journey includes roles that emphasize compliance, quality assurance, and project leadership. With over a decade of experience in the clinical research field, she has developed expertise in navigating regulatory requirements and ensuring the successful execution of clinical projects.