Hye Choi Email
Head of DDRS (Drug Development and Regulatory Strategy) JAPAC Operations @ IQVIA Asia Pacific
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Hye Choi Location
- South Korea
Hye Choi Work
- 2026 -now Head of DDRS (Drug Development and Regulatory Strategy) JAPAC Operations @
- 2022 -2026 Sr. Director Regulatory Affairs and Drug Development Solutions @
- 2021 -2026 Sr. Director Global Regulatory Affairs @
- 2020 -2021 Sr. Principal, Biopharma Integrated Development Solutions APAC @
- 2018 -2020 Principal, Strategic Clinical Development Consulting APAC @
- 2017 -2017 Head Of Consulting @ Private Consultant
- 2017 -2017 Partner, Head of Clinical Development and Regulatory Affairs @ Bridge Biotherapeutics, Inc.
- 2015 -2016 Country Head of Clinical Operations Korea and Regional Head of Global Regulatory Affairs APAC @
- 2011 -2015 Regional Head Study Start Up (SSU) and Regulatory Operations Asia Pacific @
- 2011 -2011 Regional Director ISIS North and Southeast Asia @
- 2009 -2011 Regional Manager ICON Submissions and Investigator Services (ISIS) North Asia @
- 2008 -2009 Global Project Leader HBV New Drug Development @ LG Life Sciences
- 2006 -2008 Global Project Leader Liver Diseases New Drug Development (collaboration with Gilead Sciences) @ LG Life Sciences
- 2005 -2006 Global Project Leader Osteoarthritis Medical Device Development @ LG Life Sciences
- 2002 -2004 Global Regulatory Project Manager - Antibacterial New Drug Development (collaboration with GSK) @ LG Life Sciences
- 2000 -2001 Global Project Manager New Drug Supply Chain Management @ LG Life Sciences
- 1999 -2000 Associate Manager Regulatory Affairs @
- 1997 -1998 Clinical Pharmacist @
- 1994 -1996 Research Pharmacist - Clinical Pharmacology @ Samsung Biomedical Research Institute
Hye Choi Education
- University College Dublin
Professional Certificate (International Business Management)
- 이화여자대학교
Bachelor of Pharmacy - BPharm (Clinical Pharmacy)
- International School of Hamburg (ISH)
Hye Choi Skills
- Global Regulatory Affairs (consulting, scientific advice mtgs, submissions)
- Global Product Registration
- Clinical Development and Start Up Clinical Operations
- R & D (focus on development of new molecular entities)
- New Product Roll Out
- GMP, CMC, PAI, DMF
- Alliance Management, Global Regulatory Project Management
- Licensing
- Due Diligence
- Supply Chain Management
- Clinical Pharmacology
- Clinical Pharmacy
- Pharmacotherapy
- Therapeutic Drug Monitoring
- Bioanalytical Development
- Pharmacokinetics
- Bioequivalence
- Antivirus
- Antibacterial
- Global Regulatory Project Management
- ISIS
- Pai
- Regulatory Affairs
- Scientific Advice Mtgs
- GMP
- Dmf
- CMC
- Submissions
- Global Regulatory Affairs Consulting
- R and D Focus on Development of New Molecular Entities
- Sales Management
- Icons
- PLC
- Alliance Management
- Strategic Planning
- Global Regulatory Affairs
Hye Choi Summary
- Hye Choi, based in South Korea, is currently a Head of DDRS (Drug Development and Regulatory Strategy) JAPAC Operations at IQVIA Asia Pacific. Hye Choi brings experience from previous roles at IQVIA Asia Pacific. Hye Choi holds a Professional Certificate in International Business Management @ University College Dublin. With a robust skill set that includes Global Regulatory Affairs (consulting, scientific advice mtgs, submissions), Global Product Registration, Clinical Development and Start Up Clinical Operations, R & D (focus on development of new molecular entities), New Product Roll Out and more. Hye Choi has 1 emails on RocketReach.
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