Junghee Kwon Michelet
About Junghee Kwon Michelet
Junghee Kwon Michelet is the Manager of Clinical Quality Assurance at Bristol Myers Squibb in Boudry, Neuchâtel, Switzerland. She has extensive experience in clinical quality assurance and has previously worked at Celgene, GIVENCHY, and Ilsung Corporation.
Company
Junghee Kwon Michelet is currently employed at Bristol Myers Squibb. The company is based in Boudry, Neuchâtel, Switzerland, where she serves as a Manager, Clinical Quality Assurance.
Title
Junghee Kwon Michelet holds the position of Manager, Clinical Quality Assurance at Bristol Myers Squibb. She is responsible for various quality assurance activities within the clinical domain.
Education and Expertise
Junghee Kwon Michelet has extensive educational credentials, including a Bachelor of Arts in English Language and Literature from Kyungsung University, completed over five years from 2000 to 2005. She also studied at Pacific Gateway International College, achieving a Diploma in English for one year from 2003 to 2004. Additionally, she completed a certificate in Clinical Trial Consulting in 2017, which took 11 months.
Professional Background
Throughout her career, Junghee Kwon Michelet has held various roles in different industries. At Bristol Myers Squibb, she manages Clinical Quality Assurance. Previously, she worked at Celgene in Boudry, Switzerland, as a Senior Specialist and Administrative Assistant in Clinical Quality Assurance from 2016 to 2019. Before this, she was a Sales Representative at GIVENCHY in Paris, France for six months in 2014. She also worked as an Assistant to the CEO at Ilsung Corporation in Ulsan, Korea, for seven months spanning 2012 and 2013. Her earlier roles include Receptionist positions in Melbourne, Australia, and English Teaching positions in Busan, South Korea, from 2005 to 2010.
Achievements
In her current role at Bristol Myers Squibb, Junghee Kwon Michelet has played a crucial role in the enhancement, implementation, and maintenance of the Document Management System (DMS). She provides support to eDMS end users with access requests, troubleshooting, and guidance on utilization and approval workflow. She develops KPI/scorecard presentations for stakeholders and conducts debarment checks for Principal Investigators prior to regulatory submissions. Additionally, she has contributed to the preparation, conduct, and follow-up of Health Authority GCP inspections, including dossier preparation and document quality control.