
Timeline
About me
Sr Product Data Integrity Associate at IQVIA
Education

Technological university of the shannon
2024 - 2025Postgraduate degree regulatory affair and process validation - pharmaThis postgraduate degree focused on developing expertise in current regulations, quality management systems, and effective process validation requirements. Equipped learners with the knowledge and skills to audit all or specific components of an organization’s formal Quality Management System.

Kyung hee university
2000 - 2004Bachelor's degree interior design
Experience

E-land group
Jan 2005 - Jun 2006Interior designer-Remodeled fashion floors of department stores & outlet malls (2001 outlets, New core Departments in many locations)-Managed from store layout, furniture, materials, construction details to suppliers

Youngsan glonet corp.
Jun 2007 - Apr 2008Logistics coordinator-Logistics Operation: Organizing transportation, Tracking, Settlement, etc.-Handled transportation plans and controlled trucks, oversaw the PDI (Pre Delivery Inspection) team regarding incoming cars from Glovis according to the production plan -Managed daily database -Provided interpretation of technical discussions between Korean managers and Slovak employees through English

Pantos logistics
May 2008 - Dec 2009Logistics manager-Logistics Operation: Organizing transportation, Tracking, Settlement, etc. -Integrated management of Logistics operations and administrative work-Customer Service: satisfied customer's need and demands -Interpreted between Korean managers and Polish employees through English

Emirates
Mar 2010 - Jul 2018First class-Provide a safe environment for customers through safe work practice and adequate knowledge-Perform the highest level of Customer Service on board in accordance to process and standard.-Understand, anticipate and deliver the highest level of service to all customers by availing all requests in a timely manner and maintaining integrity, confidentiality and professionalism at all times.

Iqvia
Jul 2020 - nowSenior product data integrity associate- Monitor regulatory bodies, industry sources, local specialized press, and conferences to select and integrate documents in line with the required scope, editorial, and intelligence management processes. Input regulatory documents for pharmaceuticals and medical devices.- Communicate effectively with internal and external stakeholders regarding regulatory content and documentation. Synthesize information from regulatory documentation and interactions with local country experts as needed.- Manage data efficiently and improve processes related to Regulatory Intelligence activities. Show less
Licenses & Certifications

Ielts - academic/ overall band score -7.0/ cefr level c1
British councilJun 2023
Dele a2
Instituto cervantesMay 2019
Lean practitioner (certificate of completion)
IqviaJan 2023
Peer support training certificate
EmiratesOct 2017- View certificate
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Regulatory affairs certificate: medical devices and pharmaceuticals (dual)
Regulatory affairs professionals society (raps)Apr 2024
Languages
- koKorean
- enEnglish
- spSpanish
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